Vaccine compositions comprising an amphipathic compound, a neoantigen and a hydrophobic carrier, and methods of use thereof

ABSTRACT

The present application relates to vaccine compositions comprising an amphipathic compound, a neoantigen and a hydrophobic carrier. Further described are methods and use of the vaccine composition for inducing an antibody immune response and/or a cell-mediated immune response to the neoantigen, as well as methods and uses of the vaccine compositions in the treatment of cancer.

FIELD

The present application relates to vaccine compositions comprising anamphipathic compound, a neoantigen and a hydrophobic carrier, andmethods of using such compositions in the treatment of cancer.

BACKGROUND

In immunotherapy, and cancer immunotherapy in particular, generatingsufficiently potent immune responses is a major obstacle. The immuneresponses to cancer vaccine antigens are often hampered by immunetolerance mechanisms, which originate within the tumor as a mechanism ofimmune escape (Kim 2007). Moreover, highly purified and syntheticantigens, such as peptides, are often poorly immunogenic and thusrequire immune stimulants such as adjuvants to facilitate robust immuneresponses (Irvine 2013).

Neoantigens are emerging as a very strong option to advance personalizedcancer medicine, as they have tremendous potential to effect cancertreatments that provide truly individualized immunotherapies; however,suitable delivery platforms are still required (Mullard 2016).

Neoantigens are the result of mutations in the somatic DNA of tumorsand, as such, represent a form of personalized therapy. In contrast toshared tumor antigens which are selectively expressed or over-expressedin tumors in many individuals (but still may be expressed in normalcells), neoantigens contain tumor-specific and/or patient-specificmutations and have the potential to uniquely mark a tumor fordestruction while avoiding self-tolerance.

As a result of these and other mutations or modifications, neoantigenscontain predicted epitopes (B cell and T cell) that are unique to eachpatient. Neoantigens, and the neoepitopes contained therein, may or maynot be immunogenic when injected as a vaccine, therefore selecting theappropriate formulation for immunization is crucial for ensuring optimalimmunogenicity. Additionally, since each peptide pool is unique to eachpatient, the process of identifying and then formulating the neoantigensand/or neoepitopes into an appropriate vaccine formulation within areasonable time frame is a significant consideration in respect of theirultimate use in patient therapy. Each peptide pool will containdifferent peptides with different properties which may requireoptimization, particularly if the vaccine formulation is not sufficientto handle weakly immunogenic antigens.

There remains a need for the development of optimal vaccine compositionsfor inducing strong humoral and/or cell-mediated immune responsesagainst neoantigens. In the present disclosure, we describe novelvaccine compositions for enhancing immunogenicity against neoantigens,including neoantigens which are weakly immunogenic.

SUMMARY

In an embodiment, the present invention relates to a vaccine compositioncomprising: (a) an amphipathic compound; (b) a neoantigen; and (c) ahydrophobic carrier.

In another embodiment, the vaccine composition as described herein iswater-free or substantially free of water.

In another embodiment, the present invention relates to a vaccinecomposition which comprises: (a) a lipid molecule mixture of1,2-dioleoyl-sn-glycero-3-phosphocholine (DOPC) and cholesterol; (b) aneoantigen; (c) the hydrophobic carrier Montanide® ISA 51; (d) auniversal T-helper epitope from tetanus toxoid comprising the amino acidsequence AQYIKANSKFIGITEL (A16L peptide; SEQ ID NO: 1); and (e) a DNAand/or RNA polyI:C polynucleotide adjuvant.

In another embodiment, the present invention relates to a methodcomprising administering the vaccine composition as described herein toa subject in need thereof. In an aspect of this embodiment, the methodis for inducing an antibody immune response and/or a cell-mediatedimmune response to the neoantigen in the subject. In another aspect ofthis embodiment, the method is for the treatment and/or prevention ofcancer.

In another embodiment, the method as described herein further comprisesadministering to the subject an agent that interferes with DNAreplication, such as for example cyclophosphamide.

In another embodiment, the method as described herein further comprisesadministering to the subject an immune response checkpoint inhibitor,such as for example an inhibitor of Programmed Death-Ligand 1 (PD-L1),Programmed Death 1 (PD-1), CTLA-4, PD-L2, LAG3, TIM3, 41BB, 2B4, A2aR,B7H1, B7H3, B7H4, BTLA, CD2, CD27, CD28, CD30, CD40, CD70, CD80, CD86,CD160, CD226, CD276, DR3, GALS, GITR, HVEM, IDOL IDO2, inducible T cellcostimulatory (ICOS), KIR, LAIR1, LIGHT, macrophage receptor withcollageneous structure (MARCO), phosphatidylserine (PS), OX-40, SLAM,TIGIT, VISTA, VTCN1, or any combination thereof.

In another embodiment, the present invention relates to the use of acomposition as described herein for inducing an antibody immune responseto said neoantigen in a subject.

In another embodiment, the present invention relates to the use of acomposition as described herein for inducing a cell-mediated immuneresponse to said neoantigen in a subject.

In another embodiment, the present invention relates to the use of acomposition as described herein for the treatment and/or prevention ofcancer.

In another embodiment, the present invention relates to a kitcomprising: a first container comprising an amphipathic compound and aneoantigen; and a second container comprising a hydrophobic carrier.

BRIEF BESCRIPTION OF THE FIGURES

In the figures, which illustrate embodiments of the invention by way ofexample only:

FIG. 1 illustrates the IFN-gamma ELISPOT responses of C57BL/6 VAF/Elite®Crl mice vaccinated with Mut30 antigen prepared in either an oil-basedformulation or an aqueous formulation. Immune responses were measuredeight days after vaccination by stimulating splenocytes with syngeneicdendritic cells unloaded or loaded with an irrelevant peptide or Mut 30neoantigen in an IFN-gamma ELISPOT plate. Statistical analysis wasperformed by 2-way ANOVA with Bonferroni post test comparing groupresponses to Mut30 peptide: *p<0.05, ***p<0.001.

FIG. 2 illustrates the IFN-gamma ELISPOT responses of C57BL/6 VAF/Elite®Crl mice vaccinated with Mut30 neoantigen prepared at different doses inan oil-based formulation. Immune responses were measured eight daysafter vaccination by stimulating splenocytes with syngeneic dendriticcells unloaded or loaded with an irrelevant peptide or Mut 30 neoantigenin an IFN-gamma ELISPOT plate. Statistical analysis was performed by2-way ANOVA with Bonferroni post test comparing group responses to Mut30peptide.

FIG. 3 illustrates the IFN-gamma ELISPOT responses of C57BL/6NCrl micevaccinated with Mut30 neoantigen prepared with RNA or DNA based polyI;Cmolecule in either an oil-based formulation or an aqueous bufferedformulation. Immune responses were measured eight days after vaccinationby stimulating splenocytes with syngeneic dendritic cells unloaded orloaded with an irrelevant peptide or Mut 30 neoantigen in an IFN-gammaELISPOT plate. Statistical analysis was performed by 2-way ANOVA withBonferroni post test comparing group responses to Mut30 peptide,*p<0.05, ***p<0.001.

DETAILED DESCRIPTION

One of the critical barriers in finding an effective treatment againstconstantly mutating cancer cells and epitopes has been the inability torapidly identify neoantigens (or mutated epitopes thereof), synthesizethem as peptides and manufacture these peptides in a suitableformulation to deliver as a personalized vaccine to a patient. Ideally,for a personalized medicine, this entire process could be accomplishedin about 6 to 8 weeks.

Some hurdles include, for example, (i) the absence of technologies torapidly identify neoantigens and/or their neoepitopes, (ii) theidentification of a vaccine composition that can be produced in a rapidand cost-effective manner for a production scale as small as onepatient, e.g. for personalized medicine, (iii) the identification of asuitable vaccine composition (e.g. delivery platform) that generatessufficiently strong and specific immune responses against a neoantigen,preferably after a single administration and with low doses of theneoantigen to avoid cross-reactivity, (iv) the ability of the vaccinecomposition to effectively deliver long peptide antigens (e.g. greaterthan 25 amino acids in length), (v) the identification of a vaccinecomposition that is suitable to generate an immune response (e.g. a CTLimmune response) against multiple peptide neoantigens targeting multipleepitopes across a broad range of epitopes, and (vi) the ability of thevaccine composition to induce potent immune responses to neoantigens orneoepitopes that have not been selected for their proven ability to bestrongly immunogenic and are apt to be weakly immunogenic.

In view of these hurdles, the importance of a vaccine composition havingthe ability to improve the immunogenicity of a neoantigen issignificantly greater than in traditional vaccine epitope selection.Moreover, it is desirable that the vaccine composition be capable ofinducing an effective immune response against multiple epitopes at thesame time using peptide neoantigens. It is also desirable that thevaccine composition be capable of inducing an immune response to a lowdose of the neoantigen after only a single administration, with the aimof avoiding cross-reactivity against the wild-type peptide in thesubject.

Described in the present application are vaccine compositions that arecapable of inducing potent immune responses, even in respect of weaklyimmunogenic neoantigens. Moreover, the vaccine compositions as disclosedherein should be compatible and amenable to cost-effective, scalablemanufacturing capabilities.

The oil-based compositions of the invention, comprising an amphipathiccompound; a neoantigen; and a hydrophobic carrier, were surprisinglycapable of generating statistically significant enhanced immuneresponses to a neoantigen peptide after single administration, ascompared to equivalent aqueous-based formulations.

As an exemplary neoantigen, we used the Mut30 neoantigen identified byCastle 2012. Castle 2012 purport that the Mut30 neoantigen was capableof generating strong mutation-specific immune responses in mice using anaqueous-based composition. However, Castle 2012 did not study low doseadministration of Mut30 with only a single administration, which mayrepresent important features of a successful neoantigen vaccine,particularly for weakly immunogenic neoantigens where high doses orrepeated administration could lead to cross-reactivity withself-peptides.

As shown herein, we were unable to generate strong immune responses withaqueous-based formulations comprising a Mut30 neoantigen after singleadministration. In contrast, when the Mut30 neoantigen was formulated inthe oil-based compositions of the invention, the immune responses weresignificantly enhanced. These results are shown in FIGS. 1 and 3. Theoil-based compositions of the invention were capable of generatingcell-mediated immune responses against the 27-amino acid Mut30neoantigen peptide at levels that were consistently at least about3-fold greater than with the aqueous-based formulations after a singleadministration. This is a surprising result given that neoantigens areoften weakly immunogenic peptides.

Moreover, the oil-based formulations of the invention were able togenerate these enhanced immune responses with significantly lower dosesof the neoantigen. As shown in FIG. 2, the oil-based compositions of theinvention were capable of generating comparable immune responses to theMut30 neoantigen at both high and low doses of 100 micrograms and 50micrograms, respectively. Given the similarity between neoantigens andself-peptides (e.g. single amino acid mutations), the ability to reducethe amount of neoantigen delivered, while still providing an effectiveimmune response, represents an important advantage of the presentinvention.

It is clear from the examples described herein that the compositions ofthe invention are capable of inducing unusually strong immune responsesto neoantigens, at low dose amounts after single administration.

Vaccine Compositions

In an embodiment, the present disclosure relates to a vaccinecomposition comprising an amphipathic compound, a neoantigen and ahydrophobic carrier. Each of these components is individually describedherein in greater detail. In an embodiment, the vaccine composition iswater-free or substantially free of water as described herein.

As used herein, the terms “vaccine”, “vaccine composition” or“composition” may be used interchangeably, as the context requires.

Vaccine compositions as disclosed herein may be administered to asubject in a therapeutically effect amount. As used herein, a“therapeutically effective amount” means an amount of the vaccine oractive ingredient (e.g., one or more neoantigens) effective tostimulate, induce, maintain, boost or enhance an immune response in asubject. In some embodiments, a therapeutically effective amount of thevaccine is an amount capable of inducing a clinical response in asubject in the treatment of a particular disease or disorder.Determination of a therapeutically effective amount of the vaccine iswell within the capability of those skilled in the art, especially inlight of the disclosure provided herein. The therapeutically effectiveamount may vary according to a variety of factors such as the subject'scondition, weight, sex and age.

Neoantigen

The vaccine compositions as disclosed herein comprise one or moreneoantigens.

As used herein, the term “neoantigen” refers to a class of tumorantigens which arise from tumor-specific mutations in an expressedprotein. The neoantigen can be derived from any cancer, tumor or cellthereof. The term encompasses both a neoantigenic peptide and apolynucleotide encoding a neoantigenic peptide. Thus, while the term“neoantigenic peptide” refers specifically to the peptide neoantigen,the term “neoantigen” more broadly encompasses the polynucleotide thatencodes a neoantigenic peptide.

As used herein, the term “derived from” encompasses, without limitation:an neoantigen that is isolated or obtained directly from an originatingsource (e.g. a subject); a synthetic or recombinantly generatedneoantigen that is identical in sequence to a neoantigen from anoriginating source; or a neoantigen which is made from a neoantigen ofan originating source or a fragment thereof.

The mutations in the expressed protein that create the neoantigen may bepatient-specific. By “patient-specific”, it is meant that themutation(s) are unique to an individual subject. However, it is possiblethat more than one subject will share the same mutation(s). Thus, a“patient-specific” mutation may be shared by a small or largesub-population of subjects.

In certain embodiments, the size of the neoantigenic peptide may beabout 5, about 6, about 7, about 8, about 9, about 10, about 11, about12, about 13, about 14, about 15, about 16, about 17, about 18, about19, about 20, about 21, about 22, about 23, about 24, about 25, about26, about 27, about 28, about 29, about 30, about 31, about 32, about33, about 34, about 35, about 36, about 37, about 38, about 39, about40, about 41, about 42, about 43, about 44, about 45, about 46, about47, about 48, about 49, about 50, about 60, about 70, about 80, about90, about 100, about 110, about 120 or greater amino acid residues, andany range derivable therein. In some embodiments, the neoantigenicpeptide is greater than 25 amino acids in length. In some embodiments,the neoantigenic peptide is 5 to 50 amino acids in length. In someembodiments, the neoantigenic peptide is 27 amino acids in length.

The neoantigenic peptide may comprise one or more neoepitopes. As usedherein, the term “epitope” refers to a peptide sequence which can berecognized by the immune system, specifically by antibodies, B cells orT cells. A “neoepitope” is an epitope of a neoantigenic peptide whichcomprises a tumor-specific mutation as compared to the native amino acidsequence. Generally, neoepitopes may be identified by screeningneoantigens for anchor residues that have the potential to bind patientHLA. The neoepitopes are normally ranked using algorithms, such asNetMHC, that can predict peptide binding to HLA.

A “T-cell neoepitope” is to be understood as meaning a mutated peptidesequence which can be bound by the MHC molecules of class I or II in theform of a peptide-presenting MHC molecule or MHC complex. The T-cellneoepitope should typically be one that is amenable to recognition by Tcell receptors so that a cell-mediated immune response can occur. T-cellepitopes presented by MHC class I molecules are typically peptidesbetween 8 and 15 amino acids in length, and more often between 9 and 11amino acids in length. T-cell epitopes presented by MHC class IImolecules are typically peptides between 5 and 24 amino acids in length,and more often between 13 and 17 amino acids in length. If theneoantigen is larger than these sizes, it will be processed by theimmune system into fragments of a size more suitable for interactionwith MHC class I or II molecules. Therefore, T-cell neoepitopes may bepart of a larger peptide than those mentioned above.

A “B-cell neoepitope” is to be understood as meaning a mutated peptidesequence which can be recognized by B cells and/or by antibodies. B-cellepitopes are typically at least five amino acids, more often at leastsix amino acids, still more often at least seven or eight amino acids inlength, and may be continuous (“linear”) or discontinuous(“conformational”); the latter being formed, for example, by the foldingof a protein to bring non-contiguous parts of the primary amino acidsequence into physical proximity. Linear B-cell epitopes typically varyfrom 5 to 20 amino acids in length.

In some embodiments, at least one of the neoepitopes of the neoantigenicpeptide is a patient-specific neoepitope. As used herein, by“patient-specific neoepitope”, it is meant that the mutation(s) in theneoepitope are unique to an individual subject. However, it is possiblethat more than one subject will share the same mutation(s). Thus, a“patient-specific neoepitope” may be shared by a small or largesub-population of subjects.

In an embodiment, the vaccine composition comprises at least one, atleast two, at least three, at least four, at least five, or any greaternumber of different neoantigens. In some embodiments, the vaccinecomposition comprises one, two, three, four or five differentneoantigens. By “different neoantigens”, it is broadly meant that theneoantigens do not share the exact same sequence. The neoantigenicpeptide may be from a different protein, a different tumor-specificantigen, including an over-lapping but non-identical tumor-specificantigen, or a different mutation of the same antigen. In an embodiment,each different neoantigen comprises at least one patient-specificneoepitope from the same patient.

In an embodiment, the vaccine composition comprises only one neoantigen(i.e. a single neoantigen sequence). The vaccine composition may containmultiple copies of that same neoantigen.

As is apparent from the above, neoantigenic peptides can comprise adiverse set of peptides that are unique to an individual. These peptidesmay have different solubility properties which would make them difficultto formulate in conventional types of vaccine formulations, such asaqueous buffer or emulsion type formulations. Additionally, there may bepre-existing tolerance to these peptides in the host from which theywere derived. These aspects, among others, may cause the neoantigenicpeptides to be weakly immunogenic. Therefore, it is important to deliverthem in a vaccine formulation that is capable of generating a robustimmune response, as disclosed herein.

In some embodiments, the vaccine compositions as disclosed hereincomprise neoantigens that are weakly immunogenic. The neoantigens may beweakly immunogenic for a variety of reasons, such as lack ofheterogeneity in their sequence; small size; insufficient foreignnessfor recognition by the immune system; decreased susceptibility toantigen processing and presentation, increased degradability orinsolubility, and limited neoantigen processing and presentation due totheir expression only by tumor cells. Generally, neoantigens are moresusceptible to these factors than are regular antigens.

As used herein, by “weakly immunogenic” it is meant that in conventionalvaccines (e.g. aqueous vaccines, emulsions, etc.), the neoantigens havelittle or no ability to induce, maintain and/or boost aneoantigen-specific immune response. In an embodiment, a weaklyimmunogenic neoantigen is one that has little or no ability to induce,maintain and/or boost a neoantigen-specific immune response after asingle administration of the neoantigen.

For example, in an embodiment, a weakly immunogenic neoantigen is onethat when formulated in an aqueous vaccine, is unable to sufficientlyinduce an immune response. In a more particular embodiment, a weaklyimmunogenic neoantigen is one that when formulated in an aqueousvaccine, is unable to sufficiently induce an immune response after asingle administration of the vaccine composition. These embodiments arein contrast to when the same neoantigen is formulated in a comparablevaccine composition as disclosed herein (i.e. having the samecomponents, except formulated in a hydrophobic carrier with anamphipathic compound), whereby the neoantigen is now able tosufficiently induce an immune response. In the preceding context,“sufficiently induce an immune response” means that the neoantigen isable to induce an immune response to the extent that it can provide atherapeutic effect, e.g. in the treatment of cancer.

In an embodiment, a weakly immunogenic neoantigen is one that uponexposure to the subject in an aqueous vaccine, induces no immuneresponse or induces an immune response that is at least 2-fold, 3-fold,4-fold, 5-fold, 6-fold, 7-fold, 8-fold, 9-fold, 10-fold, 15-fold,20-fold, 30-fold, 40-fold or 50-fold less efficacious as compared to theimmune response induced upon exposure to the subject in a vaccinecomposition as described herein. In an embodiment, the immune responseis measured after a single administration of the neoantigen. The immuneresponse may be measured, for example, by enzyme-linked immunospot assay(ELISPOT).

In an embodiment, a weakly immunogenic neoantigen is one that whenadministered in an aqueous vaccine is unable to provide a measurabletherapeutic benefit to the subject; whereas a measurable therapeuticbenefit can be achieved when the neoantigen is administered in acomposition as disclosed herein. In an embodiment, the measureabletherapeutic benefit may, for example, be a reduction in tumor size or anincreased cancer survival prognosis. In an embodiment, the measurabletherapeutic benefit is a reduction in tumor size of at least 25%, 50%,75%, 80%, 85%, 90%, 95% or 100%. In an embodiment, the measurabletherapeutic benefit may be detectable with a vaccine of the inventionafter only a single administration.

In an embodiment, a weakly immunogenic neoantigen is one that, whenadministered in an aqueous vaccine at a high dose amount, is lessefficacious in generating an immune response than when administered at alow dose amount in a composition of the present invention. In anembodiment, the high dose amount (as measured in mice) is at least 100micrograms, 200 micrograms, 300 micrograms, 400 micrograms, 500micrograms or more. In an embodiment, the low dose amount (as measuredin mice) is about 10 micrograms, 20 micrograms, 30 micrograms, 40micrograms, 50 micrograms, 60 micrograms or 75 micrograms or less. Theskilled person will readily appreciate equivalent or appropriate dosesin humans. In an embodiment, the low dose amount is about 75%, about70%, about 65%, about 60%, about 55%, about 50%, about 45%, about 40%,about 35%, about 30% or about 25% of the high dose amount. In anembodiment, the immune response is measured after a singleadministration of the neoantigen.

Without limitation, weakly immunogenic neoantigens may include, forexample, purified and synthetic peptide neoantigens derived fromcancer-associated antigens.

It has been postulated that weak antigenicity is a root cause of why theimmune system typically fails to control tumor growth. Many cancerantigens stimulate a weak, and thus slow, immune response that providesthe opportunity and time for tumor cells to develop immune evasionmechanisms and to ultimately gain the upper hand. In some embodiments,neoantigens may also exhibit this weak antigenicity.

For these reasons, among others, weakly immunogenic neoantigens mayrepresent a particularly suitable type of neoantigen for use in thecompositions and methods disclosed herein. In embodiment, the vaccinecompositions disclosed herein comprise a tumor-specific neoantigen thatis weakly immunogenic.

A neoantigenic peptide used to practice the invention can be isolatedfrom natural sources, be synthetic, or be a recombinantly generatedpolypeptide. Neoantigenic peptides can be recombinantly expressed invitro or in vivo. The neoantigenic peptides used to practice theinvention can be made and isolated using any method known in the art.Neoantigenic peptides used to practice the invention can also besynthesized, whole or in part, using chemical methods well known in theart. See e.g., Caruthers 1980; Horn 1980; and Banga 1995. For example,peptide synthesis can be performed using various solid-phase techniques(see e.g., Roberge 1995; Merrifield 1997); and automated synthesis maybe achieved, e.g., using the ABI 431A Peptide Synthesizer (Perkin Elmer)in accordance with the instructions provided by the manufacturer.

In an embodiment, the neoantigen may be selected from mutated somaticproteins of a cancer using selection algorithms such as NetMHC whichlook for motifs predicted to bind to MEW class I and/or MEW class IIproteins (see e.g. Example 1).

In an embodiment, the neoantigen may be derived from a mutated gene orprotein that has previously been associated with cancer phenotypes, suchas for example tumor suppressor genes (e.g. p53); DNA repair pathwayproteins (e.g. BRCA2) and oncogenes. Exemplary embodiments of geneswhich often contain mutations giving rise to cancer phenotypes aredescribed, for example, in Castle 2012. The skilled person will be wellaware of other mutated genes and/or proteins associated with cancer, andthese are available from other literature sources.

In some embodiments, the neoantigen may comprise or consist of theneoantigens disclosed by Castle 2012. Castle 2012 does not provide theactual sequences of the neoantigens, but does provide the gene ID andlocation of the mutated peptide from which the actual sequence can beidentified using e.g the Pubmed database available online from theNational Center for Biotechnology Information (NCBI).

In an embodiment, the neoantigen may be one or more of the Mut1-50neoantigens disclosed in Table 1 of Castle 2012, or a neoantigen of thesame or related protein (e.g. a human homologue). In a particularembodiment, the neoantigen may be Mut30 having the amino acid sequencePSKPSFQEFVDWENVSPELNSTDQPFL (SEQ ID NO: 2), or a neoantigen of the sameor related protein (e.g. a human homologue). Mut30 represents aneoantigen of the Kifl8b gene that was identified from somatic pointmutations in Bl6F10 murine melanoma cells. As reported by Castle 2012,KIF18B (kinesin family member 18B) is a kinesin with microtubule motoractivity and ATP and nucleotide binding that is involved in theregulation of cell division. The neoantigen has a K739N mutation. Mut30was found by Castle 2012 to induce a strong immune reactionpreferentially against the mutated peptide when administered in anaqueous formulation.

As mentioned above, the term “neoantigen” also includes a polynucleotidethat encodes a neoantigenic peptide. Nucleic acid-based vaccinationstrategies are known, wherein a vaccine composition that contains apolynucleotide is administered to a subject. The neoantigenic peptideencoded by the polynucleotide is expressed in the subject, such that theneoantigenic peptide is ultimately present in the subject, just as ifthe vaccine composition itself had contained the neoantigenic peptide.For the purposes of the present disclosure, the term “neoantigen”, wherethe context dictates, encompasses such polynucleotides that encode theneoantigenic peptide which functions as the neoantigen.

The term “polynucleotide” encompasses a chain of nucleotides of anylength (e.g. 9, 12, 18, 24, 30, 60, 150, 300, 600, 1500 or morenucleotides) or number of strands (e.g. single-stranded ordouble-stranded). Polynucleotides may be DNA (e.g. genomic DNA or cDNA)or RNA (e.g. mRNA) or combinations thereof. They may be naturallyoccurring or synthetic (e.g. chemically synthesized). It is contemplatedthat the polynucleotide may contain modifications of one or morenitrogenous bases, pentose sugars or phosphate groups in the nucleotidechain. Such modifications are well-known in the art and may be for thepurpose of e.g. improving stability of the polynucleotide.

The polynucleotide may be delivered in various forms. In someembodiments, a naked polynucleotide may be used, either in linear form,or inserted into a plasmid, such as an expression plasmid. In otherembodiments, a live vector such as a viral or bacterial vector may beused.

One or more regulatory sequences that aid in transcription of DNA intoRNA and/or translation of RNA into a polypeptide may be present. In someinstances, such as in the case of a polynucleotide that is a messengerRNA (mRNA) molecule, regulatory sequences relating to the transcriptionprocess (e.g. a promoter) are not required, and protein expression maybe effected in the absence of a promoter. The skilled artisan caninclude suitable regulatory sequences as the circumstances require.

In some embodiments, the polynucleotide is present in an expressioncassette, in which it is operably linked to regulatory sequences thatwill permit the polynucleotide to be expressed in the subject to whichthe composition of the invention is administered. The choice ofexpression cassette depends on the subject to which the composition isadministered as well as the features desired for the expressedpolypeptide.

Typically, an expression cassette includes a promoter that is functionalin the subject and can be constitutive or inducible; a ribosome bindingsite; a start codon (ATG) if necessary; the polynucleotide encoding theneoantigenic peptide; a stop codon; and optionally a 3′ terminal region(translation and/or transcription terminator). Additional sequences suchas a region encoding a signal peptide may be included. Thepolynucleotide encoding the neoantigenic peptide may be homologous orheterologous to any of the other regulatory sequences in the expressioncassette. Sequences to be expressed together with the neoantigenicpeptide, such as a signal peptide encoding region, are typically locatedadjacent to the polynucleotide encoding the protein to be expressed andplaced in proper reading frame. The open reading frame constituted bythe polynucleotide encoding the neoantigenic peptide to be expressedsolely or together with any other sequence to be expressed (e.g. thesignal peptide), is placed under the control of the promoter so thattranscription and translation occur in the subject to which thecomposition is administered.

In some embodiments, the neoantigen may be a purified neoantigen, e.g.,from about 25% to 50% pure, from about 50% to about 75% pure, from about75% to about 85% pure, from about 85% to about 90% pure, from about 90%to about 95% pure, from about 95% to about 98% pure, from about 98% toabout 99% pure, or greater than 99% pure.

The amount of neoantigen used in a single treatment with a compositionas described herein may vary depending on the type of neoantigen andcharacteristics of the subject (e.g. size, weight, age, sex, etc). Oneskilled in the art will be able to determine, without undueexperimentation, the effective amount of neoantigen to use in aparticular application. The term “effective amount” as used herein meansan amount effective, at dosages and for periods of time necessary, toachieve the desired result.

In an embodiment, the amount of neoantigen used in a single dose of acomposition as described herein may be from 0.001 to 5 mg/unit dose ofthe composition. In certain embodiments, the amount of neoantigen willbe about 0.250 mg/unit dose of the composition. In certain embodiments,the amount of neoantigen will be about 1 mg/mL of the composition.

In some embodiments, the amount of neoantigen used in a single dose of acomposition as described herein may be about 100 micrograms.

In some embodiments, the amount of neoantigen used in a single dose of acomposition as described herein may be about 50 micrograms.

As disclosed herein, it has been surprisingly found that the oil-basedcompositions of the invention are capable of generating comparableimmune responses against a neoantigenic peptide at both a low doseamount (e.g. 50 micrograms) and a high dose amount (e.g. 100micrograms), after a single administration.

In an embodiment, the compositions of the invention are for delivery ofa low dose amount of a neoantigen. As used herein, the term “low doseamount” refers to a lower dose amount of the neoantigen in a compositionof the invention that remains capable of providing a comparable immuneresponse to a higher dose amount of the same neoantigen in a compositionof the invention and/or in a conventional type of vaccine formulation,such as an aqueous buffer or emulsion type formulation.

In an embodiment, the term “low dose amount” encompasses any dose amountof the neoantigen that is less than the minimum required dose amount togenerate an immune response using an aqueous-based formulation, but issufficient to induce an immune response using a composition of theinvention.

In an embodiment, the low dose amount is about 10 micrograms, 20micrograms, 30 micrograms, 40 micrograms, 50 micrograms, 60 microgramsor 75 micrograms or less, as measured in mice. In an embodiment, the lowdose amount is about 75%, about 70%, about 65%, about 60%, about 55%,about 50%, about 45%, about 40%, about 35%, about 30% or about 25% of ahigh dose amount. The high dose amount may be a dose amount typicallyused in an aqueous-based formulation. In an embodiment, the high doseamount of the neoantigen is at least 100 micrograms, 200 micrograms, 300micrograms, 400 micrograms, 500 micrograms or more, as measured in mice.The skilled person will readily appreciate equivalent or appropriatedoses in humans based on the dosing in mice.

Amphipathic Compound

An “amphipathic compound” is a compound having both hydrophilic andhydrophobic (lipophilic) parts or characteristics. The term “amphipathiccompound” may be used interchangeably with “amphiphile” or“amphiphilic”. In some embodiments, suitable amphipathic compounds mayalso include emulsifiers such as those described herein below. Exemplaryembodiments of emulsifiers that are encompassed herein by the term“amphipathic compound” include, without limitation, polysorbates (e.g.sorbitan monooleate), mannide oleate (Arlacel™ A), lecithin, Tween™ 80,and Spans™ 20, 80, 83 and 85. The amphipathic compound can facilitatethe incorporation of vaccine components with hydrophilic affinity into ahydrophobic carrier such as an oil in the absence of water. The vaccinecomponents can include, without limitation, neoantigens and/or adjuvantsand/or other ingredients (e.g. T-helper epitopes) that can facilitatethe production of an immune response.

Without limitation, the hydrophobic portion of an amphipathic compoundis typically a large hydrocarbon moiety, such as a long chain of theform CH₃(CH₂)_(n), with n>4. The hydrophilic portion of an amphipathiccompound is usually either a charged group or a polar uncharged group.Charged groups include anionic and cationic groups. Examples of anioniccharged groups include the following (wherein the hydrophobic part ofthe molecule is represented by “R”): carboxylates: RCO₂ ⁻; sulfates:RSO₄ ⁻; sulfonates: RSO₃ ⁻; and phosphates (the charged functionality inphospholipids). Cationic charged groups include e.g. amines: RNH₃ ⁺ (“R”again representing the hydrophobic part of the molecule). Unchargedpolar groups include e.g. alcohols with large R groups, such as diacylglycerol (DAG). Amphipathic compounds may have several hydrophobicparts, several hydrophilic parts, or several of both. Proteins and someblock copolymers are examples. Steroids, cholesterol, fatty acids, bileacids, and saponins, are also amphiphiles.

There are numerous amphipathic compounds which may be used, and thevaccine compositions disclosed herein may contain a single type ofamphipathic compound or a mixture of different types of amphipathiccompounds.

In an embodiment, the amphipathic compound is a lipid. Although anyamphiphilic lipid may be used, particularly suitable lipids may includethose with at least one fatty acid chain containing at least 4 carbons,and typically about 4 to 28 carbons in length. The fatty acid chain maycontain any number of saturated and/or unsaturated bonds. The lipid maybe a natural lipid or a synthetic lipid. Non-limiting examples ofamphiphilic lipids may include phospholipids, sphingolipids,sphingomyelin, cerobrocides, gangliosides, ether lipids, sterols,cardiolipin, cationic lipids and lipids modified with poly (ethyleneglycol) and other polymers. Synthetic lipids may include, withoutlimitation, the following fatty acid constituents: lauroyl, myristoyl,palmitoyl, stearoyl, arachidoyl, oleoyl, linoleoyl, erucoyl, orcombinations of these fatty acids.

In an embodiment, the amphipathic compound is a phospholipid or amixture of phospholipids. Broadly defined, a “phospholipid” is a memberof a group of lipid compounds that yield on hydrolysis phosphoric acid,an alcohol, fatty acid, and nitrogenous base.

Phospholipids that may be used include for example, and withoutlimitation, those with at least one head group selected from the groupconsisting of phosphoglycerol, phosphoethanolamine, phosphoserine,phosphocholine (e.g. DOPC; 1,2-Dioleoyl-sn-glycero-3-phosphocholine) andphosphoinositol. In some embodiments, a mixture of DOPC and unesterifiedcholesterol may be used. In other embodiments, a mixture of Lipoid S100lecithin and unesterified cholesterol may be used. When unesterifiedcholesterol is used, the cholesterol may be used in an amount equivalentto about 10% of the weight of phospholipid (e.g. in a DOPC:cholesterolratio of 10:1 w/w or a S100 lecitin:cholesterol ratio of 10:1 w/w). Thecholesterol is used to stabilize the formation of phospholipid vesicles.If a compound other than cholesterol is used, one skilled in the art canreadily determine the amount needed.

In some embodiments, the compositions disclosed herein may compriseabout 120 milligrams of DOPC and about 12 milligrams of cholesterol.

Another common phospholipid is sphingomyelin. Sphingomyelin containssphingosine, an amino alcohol with a long unsaturated hydrocarbon chain.A fatty acyl side chain is linked to the amino group of sphingosine byan amide bond, to form ceramide. The hydroxyl group of sphingosine isesterified to phosphocholine. Like phosphoglycerides, sphingomyelin isamphipathic.

Lecithin, which also may be used, is a natural mixture of phospholipidstypically derived from chicken eggs or sheep's wool.

All of these and other phospholipids may be used in the practice of theinvention. Phospholipids can be purchased, for example, from Avantilipids (Alabastar, Ala., USA), and lipoid LLC (Newark, N.J., USA).

In an embodiment, the amphipathic compound may be substantially evenlydispersed in the hydrophobic carrier, whereby the presence of theamphipathic compound alone is sufficient to facilitate the incorporationof vaccine components with hydrophilic affinity (e.g. a neoantigen) intoa hydrophobic carrier.

In another embodiment, the amphipathic compound may be closelyassociated with the neoantigen so as to make the neoantigen miscible inthe hydrophobic carrier. By “closely associated”, it is meant that theamphipathic compound is in such proximity with the neoantigen that theneoantigen is presented in a form that it is miscible in the hydrophobiccarrier. The close association may or may not involve physicalinteraction between the neoantigen and the amphiphile. Typically, thehydrophilic part of the amphipathic compound is oriented towards thehydrophilic moieties on the neoantigen. The amphipathic compounds mayremain substantially separate from one another or they may form variousdifferent types of structures, assemblies or arrays.

Exemplary embodiments of the types of structures, assemblies or arraysthat the amphipathic compounds may form include, without limitation:single layer sheets, bilayer sheets, multilayer sheets, single layervesicular structures (e.g. micelles), bilayer vesicular structures (e.g.unilamellar or multilamellar vesicles), or various combinations thereof.By “single layer” it is meant that the amphipathic compounds do not forma bilayer, but rather remain in a layer with the hydrophobic partoriented on one side and the hydrophilic part oriented on the oppositionside. By “bilayer” it is meant that the amphipathic compounds form atwo-layered sheet, typically with the hydrophobic part of each layerinternally oriented toward the center of the bilayer with thehydrophilic part externally oriented. However, the oppositeconfiguration is also possible. The term “multilayer” is meant toencompass any combination of single and bilayer structures. The formadopted may depend upon the specific neoantigen, the specificamphipathic compound, and/or the specific hydrophobic carrier that isused.

In an embodiment, the structure, assembly or array formed by theamphipathic compound may partially or completely surround theneoantigen. As an example, the amphipathic compound may form a closedvesicular structure around the neoantigen.

In an embodiment, the vesicular structure is a single layer vesicularstructure. An example of such a structure is a micelle. A typicalmicelle in aqueous solution forms an aggregate with the hydrophilicparts in contact with the surrounding aqueous solution, sequestering thehydrophobic parts in the micelle center. In contrast, in a hydrophobiccarrier, an inverse/reverse micelle forms with the hydrophobic parts incontact with the surrounding aqueous solution, sequestering thehydrophilic parts in the micelle center. A spherical reverse micelle canpackage a neoantigen with hydrophilic affinity within its core.

In an embodiment, the vesicular structure is a micelle or aninverse/reverse micelle. Without limitation, the size of the micelles orinverse/reverse micelles range from 2 nm (20 A) to 20 nm (200 A) indiameter. In a particular embodiment, the size of the micelles orinverse/reverse micelles is about 10 nm in diameter.

In another embodiment, the vesicular structure is a bilayer vesicularstructure, such as for example, a liposome. Liposomes are completelyclosed lipid bilayer membranes containing an entrapped aqueous volume.Liposomes may be unilamellar vesicles (possessing a single bilayermembrane) or multilamellar vesicles characterized by multimembranebilayers, each bilayer may or may not be separated from the next by anaqueous layer. A general discussion of liposomes can be found inGregoriadis 1990; and Frezard 1999. Liposomes can adsorb to virtuallyany type of cell and then release an incorporated agent (e.g.neoantigen). Alternatively, the liposome can fuse with the target cell,whereby the contents of the liposome empty into the target cell.Alternatively, a liposome may be endocytosed by cells that arephagocytic.

Liposomes have been used in the preparation of compositions comprising ahydrophobic carrier as a vesicle to encapsulate antigens as well as anemulsifier to stabilize the formulation (see e.g. WO2002/038175,WO2007/041832, WO2009/039628, WO2009/146523 and WO2013/049941).Hydrophilic antigens are typically entrapped in the aqueous interior,while hydrophobic antigens can be intercalated in the lipid bilayer ordispersed in the oil phase. In another embodiment, pre-manufacturedliposomes may be used in the vaccine compositions disclosed herein.

In embodiments where the composition is water-free, one or more of thecomponents of the composition (e.g. neoantigen, adjuvant, and/orT-helper epitope) may be encapsulated in, or mixed or suspended with,liposomes in an aqueous phase; lyophilized; and then reconstituted inthe hydrophobic carrier. In such embodiments, the liposomes mayreorganize to form alternate structures in the hydrophobic carrier.

Other embodiments of bilayer and mutilayer vesicular structures include,without limitation: niosomes, transfersomes, virosomes, multilamellarvesicles (MLV), oligolamellar vesicles (OLV), unilamellar vesicles (UV),small unilamellar vesicles (SUV), medium-sized unilamellar vesicles(MUV), large unilamellar vesicles (LUV), giant unilamellar vesicles(GUV), multivesicular vesicles (MVV), single or oligolamellar vesiclesmade by reverse-phase evaporation method (REV), multilamellar vesiclesmade by the reverse-phase evaporation method (MLV-REV), stableplurilamellar vesicles (SPLV), frozen and thawed MLV (FATMLV), vesiclesprepared by extrusion methods (VET), vesicles prepared by French press(FPV), vesicles prepared by fusion (FUV), dehydration-rehydrationvesicles (DRV), and bubblesomes (BSV). The skilled artisan willrecognize that the techniques for preparing these vesicular structuresare well known in the art (see e.g. Kreuter 1994).

Hydrophobic Carrier

The compositions disclosed herein comprise a hydrophobic carrier,preferably a liquid hydrophobic substance. These compositions may bereferred to herein interchangeably as an “oil-based formulation”, an“oil-based vaccine”, an “oil-based depot vaccine”, an “oil-based depotforming vaccine”, a “hydrophobic vaccine”, a “hydrophobic composition”or a “hydrophobic vaccine composition”.

The hydrophobic carrier may be an essentially pure hydrophobic substanceor a mixture of hydrophobic substances. Hydrophobic substances that areuseful in the compositions described herein are those that arepharmaceutically and/or immunologically acceptable. The carrier istypically a liquid but certain hydrophobic substances that are notliquids at atmospheric temperature may be liquefied, for example bywarming, and may also be useful.

Oil or a mixture of oils is a particularly suitable carrier for use inthe compositions disclosed herein. Oils should be pharmaceuticallyand/or immunologically acceptable. Suitable oils include, for example,mineral oils (especially light or low viscosity mineral oil such asDrakeol® 6VR), vegetable oils (e.g., soybean oil), nut oils (e.g.,peanut oil), or mixtures thereof. Thus, in an embodiment the hydrophobiccarrier is a hydrophobic substance such as vegetable oil, nut oil ormineral oil. Animal fats and artificial hydrophobic polymeric materials,particularly those that are liquid at atmospheric temperature or thatcan be liquefied relatively easily, may also be used.

In some embodiments, the hydrophobic carrier may be, or comprise,Incomplete Freund's Adjuvant (IFA), a mineral oil-based modelhydrophobic carrier. In another embodiment, the hydrophobic carrier maybe, or comprise, a mannide oleate in mineral oil solution, such as thatcommercially available as Montanide® ISA 51 (SEPPIC, France). Whilethese carriers are commonly used to prepare water-in-oil emulsions, thepresent disclosure avoids this type of formulation by use of anamphipathic compound to suspend the components in the absence ofsubstantial quantities of water, as described herein.

Immunovaccine Inc. has developed vaccine delivery platforms referred toas VacciMax® and DepoVax™ (DPX) (see e.g. U.S. Pat. Nos. 6,793,923 and7,824,686; WO2002/038175; WO2007/041832; WO2009/039628; WO2009/043165and WO2009/146523). DPX is a lipid-in-oil formulation that can beformulated with any antigen, or mixture of antigens. Unlike water-in-oilemulsion based vaccines, which rely on oil entrapping water dropletscontaining antigen and adjuvant, DepoVax™ based formulations rely onlipids to facilitate the incorporation of antigens and adjuvantsdirectly into the oil, without the need for emulsification. Advantagesof this approach include: (1) enhancing the solubility of hydrophilicantigens/adjuvant in oil diluents which otherwise would normally havemaximum solubility in aqueous based diluents, and (2) the elimination ofcumbersome emulsification procedures prior to vaccine administration.

In some embodiments, the vaccine compositions disclosed herein maycomprise Immunovaccine Inc.'s delivery platform DepoVax™.

Other Components

The compositions disclosed herein may further comprise one or moreadditional components as are known in the art (see e.g. Remington'sPharmaceutical Sciences, Mack Publishing Company, Easton, Pa., USA 1985;and The United States Pharmacopoeia: The National Formulary (USP 24NF19) published in 1999).

In some embodiments, the vaccine compositions may additionally comprisean adjuvant, a T-helper epitope, an emulsifier and/or an excipient.

Adjuvants

In some embodiments, the vaccine compositions disclosed herein maycomprise one or more adjuvants.

A large number of adjuvants have been described and are known to thoseskilled in the art. Exemplary adjuvants include, without limitation,alum, other compounds of aluminum, Bacillus of Calmette and Guerin(BCG), TiterMax™, Ribi™, Freund's Complete Adjuvant (FCA),CpG-containing oligodeoxynucleotides (CpG ODN), lipid A mimics oranalogs, lipopeptides and polyI:C polynucleotides.

An exemplary CpG ODN is 5′-TCCATGACGTTCCTGACGTT-3′ (SEQ ID NO: 3). Theskilled person can readily select other appropriate CpG ODNs on thebasis of the target species and efficacy.

An exemplary lipopeptide includes, without limitation, Pam3Cys-SKKKK(EMC Microcollections, Germany; SEQ ID NO: 4) or variants, homologs andanalogs thereof. The Pam2 family of lipopeptides has been shown to be aneffective alternative to the Pam3 family of lipopeptides.

In some embodiments, the pharmaceutical or vaccine compositions maycomprise a polyI:C polynucleotide as an adjuvant.

PolyI:C polynucleotides are polynucleotide molecules (either RNA or DNAor a combination of DNA and RNA) containing inosinic acid residues (I)and cytidylic acid residues (C), and which induce the production ofinflammatory cytokines, such as interferon. In some embodiments, thepolyI:C polynucleotide is double-stranded. In such embodiments, they aretypically composed of one strand consisting entirely ofcytosine-containing nucleotides and one strand consisting entirely ofinosine-containing nucleotides, although other configurations arepossible. For instance, each strand may contain both cytosine-containingand inosine-containing nucleotides. In some instances, either or bothstrand may additionally contain one or more non-cytosine or non-inosinenucleotides.

In another embodiment, the polyI:C polynucleotide may be asingle-stranded molecule containing inosinic acid residues (I) andcytidylic acid residues (C). As an example, and without limitation, thesingle-stranded polyI:C may be a sequence of repeating dIdC. In aparticular embodiment, the sequence of the single-stranded polyI:C maybe a 26-mer sequence of (IC)₁₃, i.e. ICICICICICICICICICICICICIC (SEQ IDNO: 5). As the skilled person will appreciate, due to their nature (e.g.complementarity), it is anticipated that these single-stranded moleculesof repeating dIdC would naturally form homodimers, so they areconceptually similar to polyI/polyC dimers.

It has been reported that polyI:C can be segmented every 16 residueswithout an effect on its interferon activating potential (Bobst 1981).Furthermore, the interferon inducing potential of a polyI:C moleculemismatched by introducing a uridine residue every 12 repeating cytidylicacid residues (Hendrix 1993), suggests that a minimal double strandedpolyI:C molecule of 12 residues is sufficient to promote interferonproduction. Others have also suggested that regions as small as 6-12residues, which correspond to 0.5-1 helical turn of the double strandedpolynucleotide, are capable of triggering the induction process (Greene1978). If synthetically made, polyI:C polynucleotides are typicallyabout 20 or more residues in length (commonly 22, 24, 26, 28 or 30residues in length). If semi-synthetically made (e.g. using an enzyme),the length of the strand may be 500, 1000 or more residues.

PolyI:C acts as a mimic of viral genomes and is particularly useful formodulating the immune system in vivo. Synthetic poly I:poly Chomopolymers for example have been reported to enhance innate immunityby inducing interferon gamma non-specifically when deliveredsystemically in vivo by intravenous or intramuscular injection (Krown1985, Zhu 2007). Several variants of poly inosinic and cytidylic acidpolymers have been described over the years (de Clercq 1978, Bobst 1981,de Clercq 1975, Guschlbauer 1977, Fukui 1977, Johnston 1975, U.S. Pat.No. 3,906,092, Kamath 2008, Ichinohe 2007), some of which included theuse of covalently modified residues, the use of ribo and deoxy-riboinosinic and cytidylic residues, the use of homopolymers and alternatingco-polymers that contain inosinic and cytidylic acid residues, and theintroduction of specific residues to create mismatched polymers.

The use of double stranded polynucleotides containing inosinic andcytidylic acids has been reported for the treatment of a number of viraldiseases (Kende 1987, Poast 2002, U.S. Pat. No. 6,468,558, Sarma 1969,Stephen 1977, Levy 1978), cancer (Dune 1985, Salazar 1996, Theriault1986, Nakamura 1982, Talmadge 1985, Droller 1987), autoimmune diseaselike multiple sclerosis (Bever 1986), and other infectious diseases suchas malaria (Awasthi 1997, Puri 1996). The efficacy of polyI:C moleculeshas been further enhanced in some cases by complexing the molecule withpositively charged poly-lysine and carboxymethyl-cellulose, effectivelyprotecting the polynucleotide from nuclease degradation in vivo (Stephen1977, Levy 1985), or by complexing polyI:C with positively chargedsynthetic peptides (Schellack 2006).

In addition to its use as a non-specific enhancer of innate immunity,polyI:C is also useful as an adjuvant in vaccine compositions. Theenhancement of innate immunity can lead to an enhanced antigen specificadaptive immunity, possibly through a mechanism that involves, at leastin part, NK cells, macrophages and/or dendritic cells (Chirigos 1985,Salem 2006, Alexopoulou 2001, Trumpfheller 2008). Evidence for the useof polyI:C molecules in this context originates from various vaccinestudies for controlling infectious diseases (Houston 1976, Stephen 1977,Ichinohe 2007, Sloat 2008, Agger 2006, Padalko 2004) and the preventionor treatment of cancer by a variety of vaccine modalities (Zhu 2007, Cui2006, Salem 2005, Fujimura 2006, Llopiz 2008). These studies demonstratethat polyI:C enhances humoral responses as evident from enhancedantibody responses against specific infectious disease antigens. PolyI:Cis also a potentiator of antigen-specific cellular responses (Zhu 2007,Zaks 2006, Cui 2006, Riedl 2008). The adjuvanting effects of polyI:Cmolecules are believed to occur, at least partially, by inducinginterferon-gamma through their interaction with toll like receptors(TLR) such as TLR3, TLR4, TLR7, TLR8 and TLR9 (Alexopoulou 2001,Trumpfheller 2008, Schellack 2006, Riedl 2008), with TLR3 beingparticularly relevant for most polyI:C molecules. Evidence also suggeststhat polyI:C molecules may exert their effect, at least in part, byinteracting with receptors other than TLRs, such as the RNA helicaseretinoic acid induced protein I (RIG-I)/melanoma differentiationassociated gene 5 (MDA5) (Alexopoulou 2001, Yoneyama 2004, Gowen 2007,Dong 2008). The mechanism of action of polyI:C molecules remains to befully understood.

Accordingly, as used herein, a “polyI:C”, “polyI:C polynucleotide” or“polyI:C polynucleotide adjuvant” is a double- or single-strandedpolynucleotide molecule (RNA or DNA or a combination of DNA and RNA),each strand of which contains at least 6 contiguous inosinic orcytidylic acid residues, or 6 contiguous residues selected from inosinicacid and cytidylic acid in any order (e.g. IICIIC or ICICIC), and whichis capable of inducing or enhancing the production of at least oneinflammatory cytokine, such as interferon, in a mammalian subject.PolyI:C polynucleotides will typically have a length of about 8, 10, 12,14, 16, 18, 20, 22, 24, 25, 26, 28, 30, 35, 40, 45, 50, 55, 60, 65, 70,75, 80, 85, 90, 95, 100, 150, 200, 250, 300, 500, 1000 or more residues.Preferred polyI:C polynucleotides may have a minimum length of about 6,8, 10, 12, 14, 16, 18, 20, 22, 24, 26, 28, or 30 nucleotides and amaximum length of about 1000, 500, 300, 200, 100, 90, 80, 70, 60, 50, 45or 40 nucleotides.

Each strand of a double-stranded polyI:C polynucleotide may be ahomopolymer of inosinic or cytidylic acid residues, or each strand maybe a heteropolymer containing both inosinic and cytidylic acid residues.In either case, the polymer may be interrupted by one or morenon-inosinic or non-cytidylic acid residues (e.g. uridine), providedthere is at least one contiguous region of 6 I, 6 C or 6 I/C residues asdescribed above. Typically, each strand of a polyI:C polynucleotide willcontain no more than 1 non-I/C residue per 6 I/C residues, morepreferably, no more than 1 non-I/C residue per every 8, 10, 12, 14, 16,18, 20, 22, 24, 26, 28 or 30 I/C residues.

The inosinic acid or cytidylic acid (or other) residues in the polyI:Cpolynucleotide may be derivatized or modified as is known in the art,provided the ability of the polyI:C polynucleotide to promote theproduction of an inflammatory cytokine, such as interferon, is retained.Non-limiting examples of derivatives or modifications include e.g. azidomodifications, fluoro modifications, or the use of thioester (orsimilar) linkages instead of natural phosphodiester linkages to enhancestability in vivo. The polyI:C polynucleotide may also be modified toe.g. enhance its resistance to degradation in vivo by e.g. complexingthe molecule with positively charged poly-lysine andcarboxymethylcellulose, or with a positively charged synthetic peptide.

In some embodiments, the polyI:C polynucleotide adjuvant is atraditional form of polyI:C with an approximate molecular weight of989,486 Daltons, containing a mixture of varying strand lengths of polyIand polyC of several hundred base pairs (Thermo Scientific; USA).

In some embodiments, the vaccine compositions as disclosed herein maycomprise an adjuvant that activates or increases the activity of TLR2.As used herein, an adjuvant which “activates” or “increases theactivity” of a TLR2 includes any adjuvant, in some embodiments alipid-based adjuvant, which acts as a TLR2 agonist. Further, activatingor increasing the activity of TLR2 encompasses its activation in anymonomeric, homodimeric or heterodimeric form, and particularly includesthe activation of TLR2 as a heterodimer with TLR1 or TLR6 (i.e. TLR1/2or TLR2/6). Exemplary embodiments of an adjuvant that activates orincreases the activity of TLR2 include lipid-based adjuvants, such asthose described in WO2013/049941.

Thus, in an embodiment, the vaccine composition as disclosed herein maycomprise a lipid-based adjuvant, such as disclosed for example inWO2013/049941. In an embodiment, the lipid-based adjuvant isPAM2Cys-Ser-(Lys)4 (SEQ ID NO: 4) or PAM3Cys-Ser-(Lys)4 (SEQ ID NO: 4).

In another embodiment, the vaccine composition as disclosed herein maycomprise a lipid A mimic or analog adjuvant, such as for example thosedisclosed in International Patent Application No. PCT/CA2015/051309 andthe references cited therein. In a particular embodiment, the adjuvantmay be JL-265 or JL-266 as disclosed in PCT/CA2015/051309.

Further examples of adjuvants that may be used include, withoutlimitation, chemokines, colony stimulating factors, cytokines, 1018 ISS,aluminum salts, Amplivax, AS04, AS15, ABM2, Adjumer, Algammulin, ASO1B,AS02 (SBASA), ASO2A, BCG, Calcitriol, Chitosan, Cholera toxin,CP-870,893, CpG, polyI:C, CyaA, DETOX (Ribi Immunochemicals),Dimethyldioctadecylammonium bromide (DDA), Dibutyl phthalate (DBP),dSLIM, Gamma inulin, GM-CSF, GMDP, Glycerol, IC30, IC31, Imiquimod,ImuFact IMP321, IS Patch, ISCOM, ISCOMATRIX, Juvlmmune, LipoVac, LPS,lipid core protein, MF59, monophosphoryl lipid A and analogs or mimicsthereof, Montanide® IMS1312, Montanide® based adjuvants (e.g. MontanideISA-51, -50 and -70), OK-432, OM-174, OM-197-MP-EC, ONTAK, PepTel vectorsystem, other palmitoyl based molecules, PLG microparticles, resiquimod,squalene, SLR172, YF-17 DBCG, QS21, QuilA, P1005, Poloxamer, Saponin,synthetic polynucleotides, Zymosan, pertussis toxin.

Accordingly, the compositions herein may comprise one or morepharmaceutically acceptable adjuvants. In some embodiments, at least oneof the neoantigens may be coupled to at least one of the adjuvants.

In some embodiments, the compositions herein may comprise a polyI:Cpolynucleotide adjuvant, a lipid-based adjuvant, a lipid A mimic oranalog, or any combination thereof. In a particular embodiment, thecompositions may comprise a combination of a polyI:C polynucleotideadjuvant and a lipid-based adjuvant, such as described in theadjuvanting system disclosed in U.S. Provisional Patent Application No.62/256,875 filed on Nov. 18, 2015.

The amount of adjuvant used depends on the type and amount of neoantigenand on the type of adjuvant. One skilled in the art can readilydetermine the amount of adjuvant needed in a particular application byempirical testing.

T-Helper Epitopes

In some embodiments, the compositions disclosed herein may also compriseat least one T-helper epitope or T-helper antigen.

T-helper epitopes are a sequence of amino acids (natural or non-naturalamino acids) that have T-helper activity. T-helper epitopes arerecognised by T-helper lymphocytes, which play an important role inestablishing and maximising the capabilities of the immune system, andare involved in activating and directing other immune cells, such as forexample cytotoxic T lymphocytes.

A T-helper epitope can consist of a continuous or discontinuous epitope.Hence not every amino acid of a T-helper is necessarily part of theepitope. Accordingly, T-helper epitopes, including analogs and segmentsof T-helper epitopes, are capable of enhancing or stimulating an immuneresponse. Immunodominant T-helper epitopes are broadly reactive inanimal and human populations with widely divergent MHC types (Celis1988, Demotz 1989, Chong 1992). The T-helper domain of the subjectpeptides may have from about 10 to about 50 amino acids, and moreparticularly about 10 to about 30 amino acids. When multiple T-helperepitopes are present, then each T-helper epitope acts independently.

In some embodiments, the T-helper epitope may form part of a neoantigendescribed herein. In particular, if the neoantigen is of sufficientsize, it may contain an epitope that functions as a T-helper epitope. Inother embodiments, the T-helper epitope is a separate molecule from theneoantigen. In other embodiments, the T-helper epitope may be fused tothe neoantigen.

In another embodiment, T-helper epitope analogs may includesubstitutions, deletions and insertions of from one to about 10 aminoacid residues in the T-helper epitope. T-helper segments are contiguousportions of a T-helper epitope that are sufficient to enhance orstimulate an immune response. An example of T-helper segments is aseries of overlapping peptides that are derived from a single longerpeptide.

In a particular embodiment, the compositions as disclosed herein maycomprise as a T-helper epitope or antigen, the modified Tetanus toxinpeptide A16L (830 to 844; AQYIKANSKFIGITEL (SEQ ID NO: 1), with analanine residue added to its amino terminus to enhance stability(Slingluff 2001).

Other sources of T-helper epitopes which may be used in the presentcompositions include, for example, hepatitis B surface antigen helper Tcell epitopes, pertussis toxin helper T cell epitopes, measles virus Fprotein helper T cell epitope, Chlamydia trachomitis major outermembrane protein helper T cell epitope, diphtheria toxin helper T cellepitopes, Plasmodium falciparum circumsporozoite helper T cell epitopes,Schistosoma mansoni triose phosphate isomerase helper T cell epitopes,Escherichia coli TraT helper T cell epitopes and immune-enhancinganalogs and segments of any of these T-helper epitopes.

In some embodiments, the T-helper epitope may be a universal T-helperepitope. A universal T-helper epitope as used herein refers to a peptideor other immunogenic molecule, or a fragment thereof, that binds to amultiplicity of MEW class II molecules in a manner that activates T cellfunction in a class II (CD4+ T cells)-restricted manner. An example of auniversal T-helper epitope is PADRE (pan-DR epitope) comprising thepeptide sequence AKXVAAWTLKAAA (SEQ ID NO: 6), wherein X may becyclohexylalanyl. PADRE specifically has a CD4+ T-helper epitope, thatis, it stimulates induction of a PADRE-specific CD4+ T-helper response.

In addition to the modified tetanus toxin peptide A16L mentionedearlier, Tetanus toxoid has other T-helper epitopes that work in thesimilar manner as PADRE. Tetanus and diphtheria toxins have universalepitopes for human CD4+ cells (Diethelm-Okita 2000). In anotherembodiment, the T-helper epitope may be a tetanus toxoid peptide such asF21E comprising the peptide sequence FNNFTVSFWLRVPKVSASHLE (amino acids947-967; SEQ ID NO: 7).

In certain embodiments, the T-helper epitope is fused to at least one ofthe one or more neoantigens in the composition as disclosed herein (e.g.a fusion peptide).

Emulsifiers

In some embodiments, the vaccine compositions disclosed herein maycomprise one or more emulsifiers. The emulsifier may be a pureemulsifying agent or a mixture of emulsifying agents. The emulsifier(s)should be pharmaceutically and/or immunologically acceptable.

The use of an emulsifier may be of particular relevance to preparingcompositions that are water-free or substantially free of water. Forinstance, in some embodiments an emulsifier may be used to assist instabilizing the amphipathic compound, mixture of amphipathic compoundand neoantigen, or the mixture of amphipathic compound, neoantigen andother vaccine components (e.g. polyI:C and/or lipid-based adjuvant,T-helper epitope, etc.) when the amphipathic compound or mixtures areresuspended into the hydrophobic carrier. The use of an emulsifier may,for example, promote more even distribution of the amphipathic compoundor mixture in the hydrophobic carrier.

The emulsifier may be amphipathic and therefore, the emulsifier mayinclude a broad range of compounds. In some embodiments, the emulsifiermay be a surfactant, such as for example, a non-ionic surfactant.Examples of emulsifiers which may be used include polysorbates, whichare oily liquids derived from polyethylene glycolyated sorbital, andsorbitan esters. Polysorbates may include, for example, sorbitanmonooleate. Typical emulsifiers are well-known in the art and include,without limitation, mannide oleate (Arlacel™ A), lecithin, Tween™ 80,Spans™ 20, 80, 83 and 85. In an embodiment, the emulsifier for use inthe vaccine compositions is mannide oleate.

The emulsifier is generally pre-mixed with the hydrophobic carrier. Insome embodiments, a hydrophobic carrier which already contains anemulsifier may be used. For example, a hydrophobic carrier suchMontanide™ ISA 51 already contains the emulsifier mannide oleate. Inother embodiments, the hydrophobic carrier may be mixed with emulsifierbefore combining with the amphipathic compound, mixture of amphipathiccompound and neoantigen, or the mixture of amphipathic compound,neoantigen and other vaccine components (e.g. polyI:C and/or lipid-basedadjuvant, T-helper epitope, etc.).

The emulsifier is used in an amount effective to promote evendistribution of the amphipathic compound in the hydrophobic carrierand/or to assist in the formation of structures, assemblies or arraysdescribed herein. Typically, the volume ratio (v/v) of hydrophobiccarrier to emulsifier is in the range of about 5:1 to about 15:1, moreparticularly 10:1.

Water-Free Embodiments of the Compositions

In an embodiment, the vaccine compositions disclosed herein arewater-free or substantially free of water, i.e. the vaccine compositionsare not emulsions.

By “water-free” it is meant that the compositions contain no water atall. In another embodiment, the compositions may be substantially freeof water. The term “substantially free of water” is intended toencompass embodiments where the hydrophobic carrier may still containsmall quantities of water, provided that the water is present in thenon-continuous phase of the carrier. For example, individual componentsof the composition may have small quantities of bound water that may notbe completely removed by processes such as lyophilization or evaporationand certain hydrophobic carriers may contain small amounts of waterdissolved therein. Generally, compositions as disclosed herein that are“substantially free of water” contain, for example, less than about 10%,9%, 8%, 7%, 6%, 5%, 4%, 3%, 2%, 1%, 0.5%, 0.1%, 0.05% or 0.01% water ona weight/weight basis of the total weight of the carrier component ofthe composition. The compositions that still contain small quantities ofwater do not contain a sufficient amount of water such that an emulsionwould be formed.

It is contemplated that water-free vaccine compositions as disclosedherein may be capable of generating significantly higher antibody titresand more potent cell-mediated immune responses with lower doses of oneor more of the components, e.g. neoantigen, adjuvant(s), T-helperepitope, etc. This is based on the unique mechanism of action ofDepoVax™ in forcing active uptake of the vaccine components.

Without being held to any particular theory of action, it is thoughtthat when a water-free composition of the present disclosure is used,the formulation creates a strong depot that persists over several weeksallowing prolonged clearance of neoantigen and interaction of thevaccine with the immune system. In this regard, it has been reportedthat lipid-in-oil based formulations achieve peak clearance within 3weeks of immunization, and clearance continues at a slower rate over sixmonths (Brewer et al. 2014). This is in contrast to aqueous vaccineformulations which release antigens quickly over a few hours to a week;or emulsions which form a short-lived depot.

Kits and Reagents

The vaccine compositions disclosed herein are optionally provided to auser as a kit. For example, a kit of the present disclosure contains oneor more components of the compositions disclosed herein. The kit canfurther comprise one or more additional reagents, packaging material,containers for holding the components of the kit, and an instruction setor user manual detailing preferred methods of using the kit components.In an embodiment, the containers are vials.

In an embodiment, the kit contains pre-formulated vaccine in separatecontainers in a ready-to-use format. As an example, in an embodiment,the kit comprises at least one container comprising an amphipathiccompound, a neoantigen and a hydrophobic carrier. The pre-formulatedvaccine in each separate container may be the same or different.

In an alternative embodiment of the kit, the vaccine may be providedwith all components, except hydrophobic carrier, in one container (e.g.as a dry cake) ready for reconstitution in the hydrophobic carrier or asindividual components in separate containers for formulation,lyophilization and reconstitution in the hydrophobic carrier.

In an embodiment, the kit may comprise a first container comprising anamphipathic compound and a neoantigen; and a second container comprisinga hydrophobic carrier. In this embodiment, the vaccine components in thefirst container may be in the form of a dry cake that is ready to bere-suspended in the hydrophobic carrier.

In various aspects of the above kit embodiments, in addition toneoantigen, amphipathic compound and hydrophobic carrier, the vaccinemay optionally further comprise one or more of a T-helper epitope, anadjuvant, and an emulsifier. These components may be providedindividually in separate containers or may be provided as anycombination thereof together in a container, such as together in acontainer with the neoantigen and amphipathic compound.

In an embodiment of the kit, the T-helper epitope is a peptidecomprising the amino acid sequence FNNFTVSFWLRVPKVSASHLE (SEQ ID NO: 7).

In an embodiment of the kit, the T-helper epitope is a peptidecomprising the amino acid sequence AQYIKANSKFIGITEL (SEQ ID NO: 1).

In an embodiment of the kit, the adjuvant is a polyI:C polynucleotide.

In an embodiment of the kit, the amphipathic compound is one or morelipids, such as phospholipids. In an embodiment, the lipids are1,2-dioleoyl-sn-glycero-3-phosphocholine (DOPC) and cholesterol.

In an embodiment, the kit may additionally contain an agent thatinterferes with DNA replication. The agent that interferes with DNAreplication may be included in the kit in a separate container, or theagent may be included with other components. In a particular embodiment,the agent that interferes with DNA replication that is included in thekit is an alkylating agent, such as for example, cyclophosphamide.

In an embodiment, the kit may additionally contain an immune responsecheckpoint inhibitor. The immune response checkpoint inhibitor may beincluded in the kit in a separate container, or it may be included withother components. The immune response checkpoint inhibitor may be aninhibitor of Programmed Death-Ligand 1 (PD-L1), Programmed Death 1(PD-1), CTLA-4, PD-L2, LAG3, TIM3, 41BB, 2B4, A2aR, B7H1, B7H3, B7H4,BTLA, CD2, CD27, CD28, CD30, CD40, CD70, CD80, CD86, CD160, CD226,CD276, DR3, GALS, GITR, HVEM, IDO1, IDO2, inducible T cell costimulatory(ICOS), KIR, LAIR1, LIGHT, macrophage receptor with collageneousstructure (MARCO), phosphatidylserine (PS), OX-40, SLAM, TIGIT, VISTA,VTCN1, or any combination thereof.

The skilled person will appreciate that alternate arrangements of thekit are possible and are encompassed by the disclosure herein.

The kit as disclosed herein may be used in practicing the methodsdisclosed herein. In an embodiment, the kit is for use in inducing anantibody immune response and/or cell-mediated immune response to theneoantigen in a subject. In an embodiment that may be particularlysuitable, the kit is for preparing a vaccine composition that iswater-free or substantially free of water.

Immune Responses and Methods of Use

The compositions disclosed herein may find application in any instancein which it is desired to administer a neoantigen to a subject. Thesubject may be a vertebrate, such as a fish, bird or mammal, preferablya human.

As referred to herein, the “immune response” may either be acell-mediated immune response or an antibody (humoral) immune response.

In some embodiments, the vaccine compositions disclosed herein may beused for inducing a cell-mediated immune response to the neoantigen.

As used herein, to “induce” an immune response is to elicit and/orpotentiate an immune response. Inducing an immune response encompassesinstances where the immune response is enhanced, elevated, improved orstrengthened to the benefit of the host relative to the prior immuneresponse status, for example, before the administration of a compositiondisclosed herein.

As used herein, the terms “cell-mediated immune response”, “cellularimmunity”, “cellular immune response” or “cytotoxic T-lymphocyte (CTL)immune response” (used interchangeably herein) refer to an immuneresponse characterized by the activation of macrophages and naturalkiller cells, the production of neoantigen-specific cytotoxic Tlymphocytes and/or the release of various cytokines in response to aneoantigen. Cytotoxic T lymphocytes are a sub-group of T lymphocytes (atype of white blood cell) which are capable of inducing the death ofinfected somatic or tumor cells; they kill cells that are infected withviruses (or other pathogens), or that are otherwise damaged ordysfunctional.

Most cytotoxic T cells express T cell receptors that can recognise aspecific peptide antigen bound to Class I MHC molecules. Typically,cytotoxic T cells also express CD8 (i.e. CD8+ T cells), which isattracted to portions of the Class I MHC molecule. This affinity keepsthe cytotoxic T cell and the target cell bound closely together duringantigen-specific activation.

Cellular immunity protects the body by, for example, activatingantigen-specific cytotoxic T-lymphocytes (e.g. antigen-specific CD8+ Tcells) that are able to lyse body cells displaying epitopes of foreignor mutated antigen on their surface, such as cancer cells displayingtumor-specific neoantigens; activating macrophages and natural killercells, enabling them to destroy intracellular pathogens; and stimulatingcells to secrete a variety of cytokines that influence the function ofother cells involved in adaptive immune responses and innate immuneresponses.

Cellular immunity is an important component of the adaptive immuneresponse and following recognition of neoantigen by cells through theirinteraction with neoantigen-presenting cells such as dendritic cells, Blymphocytes and to a lesser extent, macrophages, protect the body byvarious mechanisms such as:

1. activating antigen-specific cytotoxic T-lymphocytes that are able toinduce apoptosis in body cells displaying epitopes of foreign or mutatedantigen on their surface, such as cancer cells displaying tumor-specificneoantigens;

2. activating macrophages and natural killer cells, enabling them todestroy intracellular pathogens; and

3. stimulating cells to secrete a variety of cytokines that influencethe function of other cells involved in adaptive immune responses andinnate immune responses.

Cell-mediated immunity is most effective in removing virus-infectedcells, but also participates in defending against fungi, protozoans,cancers, and intracellular bacteria. It also plays a major role intransplant rejection.

Since cell-mediated immunity involves the participation of various celltypes and is mediated by different mechanisms, several methods could beused to demonstrate the induction of immunity following vaccination.These could be broadly classified into detection of: i) specific antigenpresenting cells; ii) specific effector cells and their functions andiii) release of soluble mediators such as cytokines.

i) Antigen presenting cells: Dendritic cells and B cells (and to alesser extent macrophages) are equipped with special immunostimulatoryreceptors that allow for enhanced activation of T cells, and are termedprofessional antigen presenting cells (APC). These immunostimulatorymolecules (also called co-stimulatory molecules) are up-regulated onthese cells following infection or vaccination, during the process ofantigen presentation to effector cells such as CD4 and CD8 cytotoxic Tcells. Such co-stimulatory molecules (such as CD40, CD80, CD86, MHCclass I or MHC class II) can be detected, for example, by using flowcytometry with fluorochrome-conjugated antibodies directed against thesemolecules along with antibodies that specifically identify APC (such asCD11c for dendritic cells).

ii) Cytotoxic T cells: (also known as Tc, killer T cell, or cytotoxicT-lymphocyte (CTL)) are a sub-group of T cells which induce the death ofcells that are infected with viruses (and other pathogens), orexpressing tumor antigens or neoantigens. These CTLs directly attackother cells carrying certain foreign or abnormal molecules on theirsurface. The ability of such cellular cytotoxicity can be detected usingin vitro cytolytic assays (chromium release assay). Thus, induction ofadaptive cellular immunity can be demonstrated by the presence of suchcytotoxic T cells, wherein, when neoantigen loaded target cells arelysed by specific CTLs that are generated in vivo following vaccinationor infection.

Naive cytotoxic T cells are activated when their T cell receptor (TCR)strongly interacts with a peptide-bound MHC class I molecule. Thisaffinity depends on the type and orientation of the antigen/MHC complex,and is what keeps the CTL and infected cell bound together. Onceactivated the CTL undergoes a process called clonal expansion in whichit gains functionality, and divides rapidly, to produce an army of“armed”-effector cells. Activated CTL will then travel throughout thebody in search of cells bearing that unique MHC Class I+peptide. Thiscould be used to identify such CTLs in vitro by using peptide-MHC ClassI tetramers in flow cytometric assays.

When exposed to these infected or dysfunctional somatic cells, effectorCTL release perforin and granulysin: cytotoxins which form pores in thetarget cell's plasma membrane, allowing ions and water to flow into theinfected cell, and causing it to burst or lyse. CTL release granzyme, aserine protease that enters cells via pores to induce apoptosis (celldeath). Release of these molecules from CTL can be used as a measure ofsuccessful induction of cell-mediated immune response followingvaccination. This can be done by enzyme linked immunosorbant assay(ELISA) or enzyme linked immunospot assay (ELISPOT) where CTLs can bequantitatively measured. Since CTLs are also capable of producingimportant cytokines such as IFN-γ, quantitative measurement ofIFN-γ-producing CD8 cells can be achieved by ELISPOT and byflowcytometric measurement of intracellular IFN-γ in these cells.

CD4+“helper” T cells: CD4+ lymphocytes, or helper T cells, are immuneresponse mediators, and play an important role in establishing andmaximizing the capabilities of the adaptive immune response. These cellshave no cytotoxic or phagocytic activity; and cannot kill infected cellsor clear pathogens, but, in essence “manage” the immune response, bydirecting other cells to perform these tasks. Two types of effector CD4+T helper cell responses can be induced by a professional APC, designatedTh1 and Th2, each designed to eliminate different types of pathogens.

Helper T cells express T cell receptors (TCR) that recognize antigenbound to Class Il MHC molecules. The activation of a naive helper T cellcauses it to release cytokines, which influences the activity of manycell types, including the APC that activated it. Helper T cells requirea much milder activation stimulus than cytotoxic T cells. Helper T cellscan provide extra signals that “help” activate cytotoxic cells. Twotypes of effector CD4+ T helper cell responses can be induced by aprofessional APC, designated Th1 and Th2, each designed to eliminatedifferent types of pathogens. The two Th cell populations differ in thepattern of the effector proteins (cytokines) produced. In general, Th1cells assist the cell-mediated immune response by activation ofmacrophages and cytotoxic T cells; whereas Th2 cells promote the humoralimmune response by stimulation of B cells for conversion into plasmacells and by formation of antibodies. For example, a response regulatedby Th1 cells may induce lgG2a and lgG2b in mouse (IgGI and lgG3 inhumans) and favor a cell mediated immune response to a neoantigen. Ifthe IgG response to an antigen is regulated by Th2 type cells, it maypredominantly enhance the production of IgGI in mouse (IgG2 in humans).The measure of cytokines associated with Th1 or Th2 responses will givea measure of successful vaccination. This can be achieved by specificELISA designed for Th1-cytokines such as IFN-γ, IL-2, IL-12, TNF-α andothers, or Th2-cytokines such as IL-4, IL-5, IL10 among others.

iii) Measurement of cytokines: released from regional lymph nodes givesa good indication of successful immunization. As a result of neoantigenpresentation and maturation of APC and immune effector cells such as CD4and CD8 T cells, several cytokines are released by lymph node cells. Byculturing these LNC in vitro in the presence of neoantigen, aneoantigen-specific immune response can be detected by measuring releaseif certain important cytokines such as IFN-γ, IL-2, IL-12, TNF-α andGM-CSF. This could be done by ELISA using culture supernatants andrecombinant cytokines as standards.

Successful immunization may be determined in a number of ways known tothe skilled person including, but not limited to, hemagglutinationinhibition (HAIJ) and serum neutralization inhibition assays to detectfunctional antibodies; challenge studies, in which vaccinated subjectsare challenged with the associated pathogen to determine the efficacy ofthe vaccination; and the use of fluorescence activated cell sorting(FACS) to determine the population of cells that express a specific cellsurface marker, e.g. in the identification of activated or memorylymphocytes. A skilled person may also determine if immunization with acomposition as disclosed herein elicited an antibody and/or cellmediated immune response using other known methods. See, for example,Coligan et al., ed. Current Protocols in Immunology, Wiley Interscience,2007.

In an embodiment, the composition disclosed herein is capable ofgenerating an enhanced cell-mediated immune response that is at least2-fold, at least 3-fold, at least 4-fold, at least 5-fold, at least6-fold, at least 7-fold, at least 8-fold, at least 9-fold or at least10-fold greater than when the neoantigen is formulated in anaqueous-based vaccine formulation. By “aqueous-based vaccine”, it ismeant a vaccine that comprises identical components as the oil-basedformulations described herein, with the exception that the hydrophobiccarrier is replaced with an aqueous carrier and the aqueous-basedvaccine does not comprise an amphipathic compound.

In an embodiment, the composition disclosed herein is capable ofgenerating the enhanced cell-mediated immune response with only a singleadministration of the composition. Thus, in an embodiment, thecompositions disclosed herein are for delivery of the neoantigen bysingle administration.

In an embodiment, the composition disclosed herein is capable ofgenerating the enhanced cell-mediated immune response by a low doseamount of the neoantigen, wherein the low dose amount is about 50% ofthe dose amount in the aqueous-based vaccine formulation.

In some embodiments, the vaccine compositions disclosed herein may beused for inducing an antibody immune response to the neoantigen.

An “antibody immune response” or “humoral immune response” (usedinterchangeably herein), as opposed to cell-mediated immunity, ismediated by secreted antibodies which are produced in the cells of the Blymphocyte lineage (B cells). Such secreted antibodies bind to antigens,such as for example those on the surfaces of foreign substances,pathogens (e.g. viruses, bacteria, etc.) and/or cancer cells, and flagthem for destruction.

As used herein, “humoral immune response” refers to antibody productionand may also include, in addition or alternatively, the accessoryprocesses that accompany it, such as for example the generation and/oractivation of T-helper 2 (Th2) or T-helper 17 (Th17) cells, cytokineproduction, isotype switching, affinity maturation and memory cellactivation. “Humoral immune response” may also include the effectorfunctions of an antibody, such as for example toxin neutralization,classical complement activation, and promotion of phagocytosis andpathogen elimination. The humoral immune response is often aided by CD4+Th2 cells and therefore the activation or generation of this cell typemay also be indicative of a humoral immune response. The term “humoralimmune response” is used interchangeably herein with “antibody response”or “antibody immune response”.

An “antibody” is a protein comprising one or more polypeptidessubstantially or partially encoded by immunoglobulin genes or fragmentsof immunoglobulin genes. The recognized immunoglobulin genes include theκ, λ, α, γ, δ, ε and μ constant region genes, as well as myriadimmunoglobulin variable region genes. Light chains are classified aseither κ or λ. Heavy chains are classified as γ, μ, α, δ, or ε, which inturn define the immunoglobulin classes, IgG, IgM, IgA, IgD and IgE,respectively. A typical immunoglobulin (antibody) structural unitcomprises a protein containing four polypeptides. Each antibodystructural unit is composed of two identical pairs of polypeptidechains, each having one “light” and one “heavy” chain. The N-terminus ofeach chain defines a variable region primarily responsible for antigenrecognition. Antibody structural units (e.g. of the IgA and IgM classes)may also assemble into oligomeric forms with each other and additionalpolypeptide chains, for example as IgM pentamers in association with theJ-chain polypeptide.

Antibodies are the antigen-specific glycoprotein products of a subset ofwhite blood cells called B lymphocytes (B cells). Engagement ofneoantigen with antibody expressed on the surface of B cells can inducean antibody response comprising stimulation of B cells to becomeactivated, to undergo mitosis and to terminally differentiate intoplasma cells, which are specialized for synthesis and secretion ofantigen-specific antibody.

B cells are the sole producers of antibodies during an immune responseand are thus a key element to effective humoral immunity. In addition toproducing large amounts of antibodies, B cells also act asantigen-presenting cells and can present neoantigenic peptide to Tcells, such as T helper CD4 or cytotoxic CD8+ T cells, thus propagatingthe immune response. B cells, as well as T cells, are part of theadaptive immune response. During an active immune response, induced forexample by either vaccination or natural infection, antigen-specific Bcells are activated and clonally expand. During expansion, B cellsevolve to have higher affinity for the epitope. Proliferation of B cellscan be induced indirectly by activated T-helper cells, and also directlythrough stimulation of receptors, such as the TLRs.

Antigen presenting cells, such as dendritic cells and B cells, are drawnto vaccination sites and can interact with neoantigens and adjuvantscontained in a vaccine composition. Typically, the adjuvant stimulatesthe cells to become activated and the neoantigen provides the blueprintfor the target. Different types of adjuvants may provide differentstimulation signals to cells. For example, polyI:C (a TLR3 agonist) canactivate dendritic cells, but not B cells. Adjuvants such as Pam3Cys,Pam2Cys and FSL-1 are especially adept at activating and initiatingproliferation of B cells, which is expected to facilitate the productionof an antibody response (Moyle 2008; So 2012).

A humoral immune response is one of the common mechanisms for effectiveinfectious disease vaccines (e.g. to protect against viral or bacterialinvaders). However, a humoral immune response can also be useful forcombating cancer. Whereas a cancer vaccine is typically designed toproduce a cell-mediated immune response that can recognize and destroycancer cells, B cell mediated responses may target cancer cells throughother mechanisms which may in some instances cooperate with a cytotoxicT cell for maximum benefit. Examples of B cell mediated (e.g. humoralimmune response mediated) anti-tumor responses include, withoutlimitation: 1) Antibodies produced by B cells that bind to surfaceantigens (e.g. neoantigens) found on tumor cells or other cells thatinfluence tumorigenesis. Such antibodies can, for example. inducekilling of target cells through antibody-dependant cell-mediatedcytotoxicity (ADCC) or complement fixation, potentially resulting in therelease of additional antigens that can be recognized by the immunesystem; 2) Antibodies that bind to receptors on tumor cells to blocktheir stimulation and in effect neutralize their effects; 3) Antibodiesthat bind to factors released by or associated with a tumor ortumor-associated cells to modulate a signaling or cellular pathway thatsupports cancer; and 4) Antibodies that bind to intracellular targetsand mediate anti-tumor activity through a currently unknown mechanism.

One method of evaluating an antibody response is to measure the titersof antibodies reactive with a particular antigen. This may be performedusing a variety of methods known in the art such as enzyme-linkedimmunosorbent assay (ELISA) of antibody-containing substances obtainedfrom animals. For example, the titers of serum antibodies which bind toa particular neoantigen may be determined in a subject both before andafter exposure to the neoantigen. A statistically significant increasein the titer of neoantigen-specific antibodies following exposure to theneoantigen would indicate the subject had mounted an antibody responseto the neoantigen.

Without limitation, other assays that may be used to detect the presenceof an neoantigen-specific antibody include immunological assays (e.g.radioimmunoassay (RIA)), immunoprecipitation assays, and protein blot(e.g. Western blot) assays; and neutralization assays (e.g.,neutralization of viral infectivity in an in vitro or in vivo assay).

The vaccine compositions disclosed herein may be useful for treating orpreventing diseases and/or disorders ameliorated by a cell-mediatedimmune response or a humoral immune response. The vaccines may findapplication in any instance in which it is desired to administer aneoantigen to a subject to induce a cell-mediated immune response or ahumoral immune response. In an embodiment, the vaccines may findapplication for the delivery of a personalized vaccine.

In an embodiment, the present disclosure relates to a method comprisingadministering the composition as described herein to a subject in needthereof. In some embodiments, the method is for inducing an antibodyimmune response and/or cell-mediated immune response to a neoantigen insaid subject. In some embodiments, the method is for the treatmentand/or prevention of cancer.

“Treating” or “treatment of”, or “preventing” or “prevention of”, asused herein, refers to an approach for obtaining beneficial or desiredresults. Beneficial or desired results can include, but are not limitedto, alleviation or amelioration of one or more symptoms or conditions,diminishment of extent of disease, stabilisation of the state ofdisease, prevention of development of disease, prevention of spread ofdisease, delay or slowing of disease progression (e.g. suppression),delay or slowing of disease onset, conferring protective immunityagainst a disease-causing agent and amelioration or palliation of thedisease state. “Treating” or “preventing” can also mean prolongingsurvival of a patient beyond that expected in the absence of treatmentand can also mean inhibiting the progression of disease temporarily orpreventing the occurrence of disease, such as by preventing infection ina subject. “Treating” or “preventing” may also refer to a reduction inthe size of a tumor mass, reduction in tumor aggressiveness, etc.

In an embodiment, the methods and compositions disclosed herein may befor use in treating and/or preventing cancer in a subject in needthereof. The subject may have cancer or may be at risk of developingcancer.

As used herein, the terms “cancer”, “cancer cells”, “tumor” and “tumorcells”, (used interchangeably) refer to cells that exhibit abnormalgrowth, characterized by a significant loss of control of cellproliferation or cells that have been immortalized. The term “cancer” or“tumor” includes metastatic as well as non-metastatic cancer or tumors.A cancer may be diagnosed using criteria generally accepted in the art,including the presence of a malignant tumor.

Without limitation, cancers that may be capable of being treated and/orprevented by the use or administration of a composition as disclosedherein include carcinoma, adenocarcinoma, lymphoma, leukemia, sarcoma,blastoma, myeloma, and germ cell tumors. Without limitation,particularly suitable embodiments may include glioblastoma, multiplemyeloma, ovarian cancer, breast cancer, fallopian tube cancer, prostatecancer or peritoneal cancer. In one embodiment, the cancer may be causedby a pathogen, such as a virus. Viruses linked to the development ofcancer are known to the skilled person and include, but are not limitedto, human papillomaviruses (HPV), John Cunningham virus (JCV), Humanherpes virus 8, Epstein Barr Virus (EBV), Merkel cell polyomavirus,Hepatitis C Virus and Human T cell leukaemia virus-1 The cancer is onethatexpresses one or more tumor-specific neoantigens.

In a particular embodiment, the cancer is breast cancer, ovarian cancer,prostate cancer, fallopian tube cancer, peritoneal cancer, glioblastomaor diffuse large B cell lymphoma.

The methods and compositions disclosed herein may be useful for eitherthe treatment or prophylaxis of cancer; for example, a reduction of theseverity of cancer (e.g. size of the tumor, aggressiveness and/orinvasiveness, malignancy, etc) or the prevention of cancer recurrences.

In an embodiment, the method for treating and/or preventing cancer firstcomprises identifying one or more neoantigens or neoepitopes in thepatients' tumor cells. The skilled person will understand methods knownin the art that can be used to identify the one or more neoantigens(see, for example, Srivastava 2015 and the references cited therein). Asan exemplary embodiment, whole genome/exome sequencing may be used toidentify mutated neoantigens that are uniquely present in a tumor of anindividual patient. The collection of identified neoantigens can beanalyzed to select (e.g. based on algorithms) a specific, optimizedsubset of neoantigens and/or neoepitopes for use as a personalizedcancer vaccine.

Having identified and selected one or more neoantigens, one of skill inthe art will appreciate that there are a variety of ways in which toproduce such neoantigens either in vitro or in vivo. The neoantigenicpeptides may be produced by any method known the art and then may beformulated into a vaccine composition or kit as described herein andadministered to a subject.

In an embodiment, upon administration to a subject, the vaccinecomposition induces a tumor-specific immune response in the treatment ofcancer. By this it is meant that the immune response specificallytargets the tumor cells without a significant effect on normal cells ofthe body which do not express the neoantigen. Further, in an embodiment,the composition may comprise at least one patient-specific neoepitopesuch that the tumor-specific immune response is patient-specific for thesubject or a subset of subjects, i.e. a personalized immunotherapy.

The vaccine composition as disclosed herein may be administered by anysuitable route. In an embodiment, the route of administration issubcutaneous injection.

Agent that Interferes with DNA Replication

The methods disclosed herein may also comprise administering an agentthat interferes with DNA replication. In a particular embodiment, anagent that interferes with DNA replication is administered when themethods disclosed herein are used in the treatment or prevention ofcancer.

Exemplary embodiments of such agents and methods of use thereof aredescribed, for example, in WO2014/153636.

As used herein, the expression “interferes with DNA replication” isintended to encompass any action that prevents, inhibits or delays thebiological process of copying (i.e., replicating) the DNA of a cell. Theskilled person will appreciate that there exist various mechanisms forpreventing, inhibiting or delaying DNA replication, such as for exampleDNA cross-linking, methylation of DNA, base substitution, etc. Themethods according to the invention encompass the use of any agent thatinterferes with DNA replication by any means known in the art. In anexemplary embodiment, and without limitation, the agent that interfereswith DNA replication is a drug.

In an embodiment, the agent that interferes with DNA replication is onewhich, when used at doses that are non-chemotherapeutic, is capable ofselectively affecting DNA replication in cells of the immune system,with the intent of modulating the immune system to enhance vaccineresponses. By “non-chemotherapeutic”, it is meant that the dose of theagent is a dose lower than that which would be used to directly andselectively destroy malignant or cancerous cells and tissues.

Other embodiments of an agent that interferes with DNA replicationinclude agents that interfere with DNA replication to cause programmedcell death, with the ability to selectively target rapidly dividingcells of the immune system. The purpose of such agents is to modulatecells of the immune system to enhance vaccine responses. Such agents aretypically used at doses that are not expected to be chemotherapeutic andare considered acceptable for use in humans. The purpose of selectivelytargeting immune cells may be to reduce the number of immune suppressivecells, and/or deplete useful immune cells involved in mediating theimmune response for the purposes of inducing rapid proliferation uponremoval of the drug targeting DNA replication.

Interference with DNA replication leading to cell death may be caused bynumerous mechanisms, including but not limited to, the formation of DNAcross-linking (e.g. by alkylating agents, platinum compounds, etc.),methylation of DNA (i.e. by methylating agents), base substitution (i.e.by nucleoside analogs). Exemplary agents and their mechanisms aredescribed in Cancer Chemotherapy and Biotherapy: Principles and Practice(Cabner B. A., 5^(th) edition, Lippincott Williams & Wilkins, PA, USA,2011).

In an embodiment, the agent that interferes with DNA replication is analkylating agent. Alkylating agents include, but are not limited to,cyclophosphamide, temozolomide, ifosfamide, mafosfamide, melphalan,busulfan, bendamustine, uramustine, carmustine orbis-chloroethylnitrosourea (BCNU), chlorambucil, mitomycin C, and theirderivatives, active metabolites or metabolite intermediates. A suitablederivative may be, for example and without limitation, palifosfamide(e.g. a derivative of ifosfamide).

In another embodiment, the agent that interferes with DNA replication isa platinum compound. Platinum compounds include, but are not limited to,carboplatin, cisplatin, oxaliplatin and their derivatives.

In another embodiment, the agent that interferes with DNA replication isa methylating agent. Methylating agents include, but are not limited to,temzolomide, procarbazine and dacarbazine, and their derivatives.

In another embodiment, the agent that interferes with DNA replication isa nucleoside analog. Non-limiting examples of nucleoside analogs includegemcitabine, 5-fluorouracil, cytosine arabinoside (Ara-C) and theirderivatives.

In another embodiment, any drug that inhibits DNA replication indirectlyby inhibiting enzymes critical to DNA replication, such as topoisomeraseI, topoisomerase II or DNA polymerase, may also be used. Such drugsinclude, for example and without limitation, doxorubicin, daunorubicin,mitoxantrone, etoposide, teniposide, topotecan, camptothecin,irinotecan, acyclovir and ganciclovir.

Exemplary agents that interfere with DNA replication, and which may beused in the methods of the invention include, without limitation, thoselisted below in Table 1. As the skilled person will appreciate, theseare examples of agents that may be used. Additional agents include, forexample, any drug or compound that interferes with DNA replication by asimilar mechanism and/or that has a similar functional group.

TABLE 1 DNA Replication Inhibitor Functional group Description ExemplaryAgents Alkylating agents Nitrogen mustard Alkylate DNA Cyclophosphamide(bischloroethylamine) Ifosfamide RN(CH₂CH₂Cl)₂ Mafosfamide MelphalanBendamustine Uramustine Palifosfamide Chlorambucil4-Hydroxycyclophosphamide Alkylating agents Nitrosourea Alkylate DNABis-chloroethylnitrosourea (BCNU)

Alkylating agents Alkyl sulfonates Alkylate DNA Busulfan

Antitumor Aziridines or Ethylene Alkylate DNA Mitomycin C Antibioticsimines and Intercalate DNA

Yondelis

Methylating Agents Reactive N-methyl Methylate DNA Procarbazine groupDacarbazine Temozolomide

Platinum Pt(II) Covalently binds Cisplatin compounds to DNA CarboplatinOxaliplatin Nucleoside analogs Resemble purine or Incorporate intoAcyclovir pyrimidine bases DNA during Gemcitabine replication5-fluorouracil Cytosine arabinoside Ganciclovir Camptothecin Quinolinealkaloids Inhibits activity Camptothecin derivatives of topoisomerase I

Topotecan Irinotecan Anthracycline Anthracycline Inhibit activity ofDoxorubicin derivatives antibiotics topoisomerase II

Daunorubicin Epirubicin Idarubicin Epipodophyllotoxin EpipodophyllotoxinInhibit activity of Etoposide derivatives topoisomerase II TeniposideAnthracenedione Anthracenedione Intercalate DNA Mitoxantrone derivativesPixantrone

In a particular embodiment, the agent that interferes with DNAreplication is a nitrogen mustard alkylating agent, or any intermediaryor active metabolite thereof. Nitrogen mustards are non-specific DNAalkylating agents. Nitrogen mustards form cyclic aminium ions(aziridinium rings) by intramolecular displacement of the chloride bythe amine nitrogen. This azidirium group is then capable of alkylatingDNA by attacking the N-7 nucleophilic center on the guanine base. Upondisplacement of the second chlorine, a second alkylation step occursthat results in the formation of interstrand cross-links (ICLs). Theselesions are highly cytotoxic since they block fundamental metabolicprocesses such as DNA replication and transcription.

The methods of the invention encompass the use of any such non-specificnitrogen mustard DNA alkylating agents. Particularly suitable nitrogenmustard alkylating agents may include for example, and withoutlimitation, cyclophosphamide, palifosfamide, bendamustine, andifosfamide.

Ifosfamide is a nitrogen mustard alkylating agent. The IUPAC name forifosfamide isN-3-bis(2-chloroethyl)-1,3,2-oxazaphosphinan-2-amide-2-oxide. Ifosfamideis commonly known as Ifex®. The chemical structure of ifosfamide is:

Palifosfamide is an active metabolite of ifosfamide that is covalentlylinked to the amino acid lysine for stability. Palifosfamideirreversibly alkylates and cross-links DNA through GC base pairs,resulting in irreparable 7-atom inter-strand cross-links; inhibition ofDNA replication and/or cell death. Palifosfamide is also known asZymafos®.

Bendamustine is another nitrogen mustard alkylating agent. The IUPACname for Bendamustine is4-[5-[Bis(2-chloroethyl)amino]-1-methylbenzimidazol-2-yl]butanoic acid,and it is commonly referred to as Treakisym®, Ribomustin®, Levact® andTreanda®. The chemical structure of bendamustine is:

Also encompassed by the methods of the invention is the use ofintermediary and/or active metabolites of DNA alkylating agents, andparticularly intermediary and/or active metabolites of the nitrogenmustard DNA alkylating agents described herein. Such metabolitesinclude, without limitation, aldophosphamide, 4-hydroxycyclophosphamide,4-hydroxyifosfamide, chloracetaldehyde and phosphamide mustard.

In a further embodiment, the agent that interferes with DNA replicationmay be any suitable pharmaceutically acceptable salt, ester, tautomer,stereoisomer, racemic mixture, solvate, hydrate or prodrug of thealkylating agents, platinum compounds, methylating agents, or nucleosideanalogs described herein.

In a particular embodiment, the agent that interferes with DNAreplication for use in the methods of the invention is cyclophosphamide.Cyclophosphamide (N,N-bis(2-chloroethyl)-1,3,2-oxazaphosphinan-2-amine2-oxide), also known as cytophosphane, is a nitrogen mustard alkylatingagent. The chemical structure of cyclophosphamide is:

Cyclophosphamide is also known and referred to under the trade-marksEndoxan®, Cytoxan®, Neosar®, Procytox® and Revimmune®. Other nitrogenmustard alkylating agents in the same class as cyclophosphamide include,without limitation, palifosfamide, bendamustine and ifosfamide.

Cyclophosphamide (CPA) is a prodrug which is typically administered viaintravenous infusion, but also can be administered parenterally andorally (de Jonge 2005) with little difference in bioavailability (Duma1979). CPA is converted to its active metabolites, 4-hydroxy-CPA andaldophosphamide, by oxidation by P450 enzymes in the liver (Emmenegger2007, Emmenegger 2011). The active metabolites of CPA are lipid solubleand enter cells through passive diffusion. Intracellular 4-OH-CPAspontaneously decomposes into phosphoramide mustard which is theultimate active metabolite. Phosphoramide mustard catalyzes intra- andinterstrand DNA cross-links as well as DNA-protein cross-links thatinhibit DNA replication leading to cell death (de Jonge 2005).Phosphoramide mustard is eliminated by enzymatic conversion tocarboxyphoshphamide by cytoplasmic aldehyde dehydrogenase (ALDH)(Emmenegger 2007, Emmenegger 2011).

Cells with low levels of ALDH tend to accumulate CPA metabolites and aremore sensitive to its effects, and indeed tumor upregulation of ALDH isone mechanism of CPA resistance (Zhang 2005). Besides ALDH, lowintracellular ATP levels have also been associated with CPA selectivitytowards particular cells types (Zhao 2010). At high doses, typically inthe range of 1-5 g/m², the effects of CPA are most cytotoxic to rapidlydividing cells indiscriminate of cell type, and CPA is myelosuppressivesince most hematogenic cells are rapidly dividing (Bruce 1996; Smith1985).

Total systemic clearance of CPA and its metabolites varies between 5-9hours, and peak plasma levels of the parent also vary considerablybetween patients (3-11 hours) reflecting genetic differences inmetabolism from person to person (Cohen 1971; Mouridsen 1974). Repeatedadministration of CPA is reported to shorten elimination half-life byincreasing activity of enzymes involved in metabolism (D'Incalci 1979),but whether this leads to increased metabolism of the active metaboliteis not known (de Jonge, Huitema et al. 2005), particularly at low doses(Emmenegger 2007).

Dose translation from human to murine studies is calculated using thefollowing equation:

Human  dose  (mg/kg) = Animal  Km Animal  dose  (mg/kg) = Human  Km

Where the constant mouse Km value is 3 and human Km value is 37(Reagan-Shaw, Nihal et al. 2008).

In the last two decades, low dose CPA has been appreciated for itsimmune modulatory and anti-angiogenic effects. In contrast to high doseCPA, low doses of CPA, typically 100-300 mg/m², lack widespreadcytotoxic activity but do appear to enhance immune-mediated tumorelimination by selectively modulating cells of the immune system andalso by reducing angiogenesis within the tumor microenvironment. Themechanisms of action and uses of low dose CPA are further described, forexample, in WO2014/153636.

In an embodiment, the methods disclosed herein comprise administering anagent that interferes with DNA replication.

The agent that interferes with DNA replication is typically administeredin an amount sufficient to provide an immune-modulating effect. As usedherein, the expression “immune-modulating effect” refers to the abilityof the agent that interferes with DNA replication to alter (modulate)one or more aspects of the immune system and/or cells of the immunesystem. In an embodiment, the “amount sufficient to provide animmune-modulating effect” is an amount of the agent that is capable ofselectively affecting DNA replication in cells the immune system. Forexample, the amount of agent may be an amount sufficient to selectivelytarget rapidly dividing cells of the immune system to cause programmedcell death.

The “amount sufficient to provide an immune-modulating effect” mayinterchangeably be referred to herein as a “low dose” amount. As relatesto a particular embodiment of the invention where the agent thatinterferes with DNA replication is the alkylating agentcyclophosphamide, the expression “low dose” typically refers to a doseof cyclophosphamide that is less than or equal to 300 mg/m², such as forexample 25-300 mg/m² and more particularly 100-300 mg/m². In anembodiment, the low dose amount of cyclophosphamide is 10, 25, 50, 75 or100 mg BID (two times daily). In a particular embodiment, the low doseamount of cyclophosphamide is 50 mg BID. The “low dose” amounts of otheragents that interfere with DNA replication, as encompassed herein, wouldbe known to those skilled in the art, or could be determined by routineskill.

In a particular embodiment, the methods disclosed herein comprise acycle of low dose metronomic cyclophosphamide. For purposes of thepresent disclosure, “metronomic” is meant to refer to a frequentadministration of a lower than normal dose amount of the agent thatinterferes with DNA replication (e.g. cyclophosphamide). As used herein,the term “normal dose amount” may refer, for example and withoutlimitation, to either: (i) the established maximum tolerated dose (MTD)or standard dose via a traditional dosing schedule, or (ii) in instanceswhere a low dose single bolus amount has been established for aparticular agent that interferes with DNA replication, than to that lowdose amount.

In metronomic dosing, the same, lower, or higher cumulative dose over acertain time period as would be administered via a traditional dosingschedule may ultimately be administered. In a particularly suitableembodiment, this is achieved by extending the time frame during whichthe dosing is conducted and/or increasing the frequency ofadministrations, while decreasing the amount administered as compared tothe normal dose amount. For example, where a low dose amount of 300mg/m² of an agent that interferes with DNA replication is typicallyadministered (e.g. by single bolus injection), a metronomic regimen maycomprise administering the same amount over a period of several days byadministering frequent low doses.

In an embodiment of the methods disclosed herein, metronomic treatmentwith the agent that interferes with DNA replication (e.g.cyclophosphamide) is intended to encompass a daily low doseadministration of the agent over a certain period of time, such as forexample a period of 2, 3, 4, 5, 6 or 7, or more, consecutive days.During these days of metronomic dosing, the agent that interferes withDNA replication may be provided at frequent regular intervals or varyingintervals. For example, in an embodiment, a dose of the agent thatinterferes with DNA replication may be administered every 1, 2, 3, 4, 6,8, 12 or 24 hours. In another embodiment, a dose of the agent thatinterferes with DNA replication may be administered once every 2, 3, or4 days. In a particular embodiment, a dose of the agent that interfereswith DNA replication may be administered two times daily.

In some embodiments, there may be breaks or gaps in the periods ofmetronomic treatment with the agent that interferes with DNAreplication. In this manner, metronomic treatment may occur in a cyclicfashion, alternating between on and off periods of administration.Particularly suitable are intervals where the agent that interferes withDNA replication is administered to the subject daily on alternatingweekly intervals. For instance, a one week period of administration ofthe agent that interferes with DNA replication is followed by a one weeksuspension of treatment, and the cycle repeats.

In an embodiment therefore, the methods disclosed herein compriseadministering the agent that interferes with DNA replication to thesubject daily for a period of 7 consecutive days, beginning every secondweek. In a particular aspect of this embodiment, the administration ofthe agent that interferes with DNA replication begins about 7 days priorto the first administration of the depot-forming vaccine. In a furtheraspect of this embodiment, the agent that interferes with DNAreplication may be administered at a dose of 50 mg BID (two times daily)on each day of administration.

In an embodiment of the methods disclosed herein, the agent thatinterferes with DNA replication may be administered as a priming agentduring the intermittent period between each administration of thedepot-forming vaccine and/or non-depot-forming vaccine.

As the skilled person will appreciate, the frequency and duration of theadministration of the agent that interferes with DNA replication, aswell as the administration of the depot-forming and non-depot-formingvaccines, may be adjusted as desired for any given subject within theparameters described above. Factors that may be taken into accountinclude, e.g.: the nature of the one or more neoantigens in the vaccine;the type of disease or disorder; the age, physical condition, bodyweight, sex and diet of the subject; and other factors.

The agent that interferes with DNA replication may be administered byany suitable delivery means and any suitable route of administration. Inan embodiment, the agent that interferes with DNA replication isadministered orally, such as in the form of a pill, tablet or capsule.In an alternate embodiment, the agent is administered by injection (e.g.intravenous). In a particular embodiment of the methods disclosedherein, the agent is cyclophosphamide and it is administered orally.

In a particular embodiment of the methods disclosed herein, the agentthat interferes with DNA replication is cyclophosphamide.

Checkpoint Inhibitor

The methods disclosed herein may also comprise administering an immuneresponse checkpoint inhibitor.

As used herein, an “immune response checkpoint inhibitor” refers to anycompound or molecule that totally or partially reduces, inhibits,interferes with or modulates one or more checkpoint proteins. Checkpointproteins regulate T-cell activation or function. Numerous checkpointproteins are known, such as for example CTLA-4 and its ligands CD80 andCD86; and PD-1 and its ligands PD-L1 and PD-L2. Checkpoint proteins areresponsible for co-stimulatory or inhibitory interactions of T-cellresponses. Checkpoint proteins regulate and maintain self-tolerance andthe duration and amplitude of physiological immune responses. Herein,the term “immune response checkpoint inhibitor” may be usedinterchangeably with “checkpoint inhibitor”.

In some embodiments, the immune response checkpoint inhibitor is aninhibitor of Programmed Death-Ligand 1 (PD-L1, also known as B7-H1,CD274), Programmed Death 1 (PD-1, CD279), CTLA-4 (CD154), PD-L2 (B7-DC,CD273), LAG3 (CD223), TIM3 (HAVCR2, CD366), 41BB (CD137), 2B4, A2aR,B7H1, B7H3, B7H4, BTLA, CD2, CD27, CD28, CD30, CD40, CD70, CD80, CD86,CD160, CD226, CD276, DR3, GALS, GITR, HVEM, IDO1, IDO2, ICOS (inducibleT cell costimulator), KIR, LAIR1, LIGHT, MARCO (macrophage receptor withcollageneous structure), PS (phosphatidylserine), OX-40, SLAM, TIGIT,VISTA, VTCN1, or any combination thereof.

In some embodiments, the immune response checkpoint inhibitor is aninhibitor of PD-L1, PD-1, CTLA-4 or any combination thereof.

In some embodiments, the immune response checkpoint inhibitor is aninhibitor of PD-L1 or PD-1. In an embodiment, the inhibitor of PD-L1 orPD-1 may be an anti-PD-1 or anti-PD-L1 antibody, such as for example andwithout limitation, those disclosed in WO 2015/103602. For example, inan embodiment, the anti-PD-1 antibody or anti-PD-L1 antibody may beselected from: nivolumab, pembrolizumab, pidilizumab, BMS-936559 (seeClinicalTrials.gov; Identifier NCT02028403), MPDL3280A (Roche, seeClinicalTrials.gov; Identifier NCT02008227), MDX1105-01 (Bristol MyersSquibb, see ClinicalTrials.gov; Identifier NCT00729664), MEDI4736(MedImmune, see ClinicalTrials.gov; Identifier NCT01693562), and MK-3475(Merck, see ClinicalTrials.gov; Identifier NCT02129556). In anembodiment, the anti-PD-1 antibody may be RMP1-4 or J43 (BioXCell) or ahuman or humanized counterpart thereof.

In some embodiments, the immune response checkpoint inhibitor is aninhibitor of CTLA-4. In an embodiment, the inhibitor of CTLA-4 may be anantibody, such as for example and without limitation, ipilimumab(Bristol-Myers Squibb) or BN13 (BioXCell). In another embodiment, theanti-CTLA-4 antibody may be UC10-4F10-11, 9D9 or 9H10 (BioXCell) or ahuman or humanized counterpart thereof.

The one or more immune response checkpoint inhibitors may beadministered by any suitable route. In some embodiments, the route ofadministration of the one or more immune response checkpoint inhibitorsis parenteral, mucosal, oral, sublingual, transdermal, topical,inhalation, intranasal, aerosol, intraperitoneal, intratumoral,intraocular, intratracheal, intrarectal, intragastric, vaginal, by genegun, dermal patch or in eye drop or mouthwash form. In an embodiment,the immune response checkpoint inhibitor may be administered bysubcutaneous injection.

As the skilled person will appreciate, the frequency and duration of theadministration of the immune response checkpoint inhibitor may beadjusted as desired for any given subject. Factors that may be takeninto account include, e.g.: the nature and type of the specificcheckpoint inhibitor; the nature of the one or more neoantigens in thevaccine; the type of disease or disorder; the age, physical condition,body weight, sex and diet of the subject; and other factors.

In some embodiments, the one or more immune response checkpointinhibitors may be administered before, after or concurrently with thedepot-forming vaccine and/or non-depot-forming vaccine. In anembodiment, the immune response checkpoint inhibitor may be administeredat a time subsequent to the first administration with the depot-formingvaccine. In aspects of this embodiment, the immune response checkpointinhibitor may be administered at a time before or after the firstadministration of the non-depot-forming vaccine.

In an embodiment, administration of the immune response checkpointinhibitor may begin on the same day as the first administration of thedepot-forming vaccine and may be administered at a desired schedulethereafter. In an embodiment, the desired schedule may be administrationof the immune response checkpoint inhibitor every 1, 2, 3, 4, 6, 8, 12or 18 hours; every 1, 2, 3, 4, 5 or 6 days; or every 1, 2, 3 or 4 weeks.In an embodiment, the desired schedule may be once every 3 days.

There may be breaks or gaps in the periods of administration of theimmune response checkpoint inhibitor. In this manner, administration mayoccur in a cyclic fashion, alternating between on and off periods ofadministration.

Methods for Preparing the Vaccine Compositions

The vaccine compositions may be prepared by known methods in the arthaving regard to the present disclosure. Exemplary embodiments forpreparing the vaccine compositions disclosed herein are described below,without limitation.

As used in this section, the term “neoantigen” is used generally todescribe how a neoantigen may be formulated in the vaccine compositionsof the present disclosure. The term “neoantigen” encompasses both thesingular form “neoantigen” and the plural “neoantigens”. It is notnecessary that all neoantigens be introduced into the vaccinecomposition in the same way.

In an embodiment for preparing the vaccine composition, the neoantigenand optionally other vaccine components (e.g. adjuvant, T-helperepitope, etc.) are reconstituted in a suitable solvent together with anamphipathic compound. The vaccine components are then dried to form adry cake, and the dry cake is resuspended in a hydrophobic carrier. Thestep of drying may be performed by various means known in the art, suchas by freeze-drying, lyophilization, rotary evaporation, evaporationunder pressure, etc. Low heat drying that does not compromise theintegrity of the components can also be used. Heat can also be used toassist in resuspending the neoantigen/amphipathic compound mixture.

The “suitable solvent” is one that is suitable for solubilizing theneoantigen, adjuvants and/or amphipathic compound, and can be determinedby the skilled person. In an embodiment, sodium phosphate buffer (0.2M,pH 6.0) or sodium phosphate buffer (0.1M, pH 7.0) may be used. In anembodiment, acetate buffer (0.1M, pH 9.5) may be used. In anotherembodiment, a polar protic solvent such as an alcohol (e.g.tert-butanol, n-butanol, isopropanol, n-propanol, ethanol or methanol),water, acetate buffer, formic acid or chloroform may be used. In somecases, the same solvent can be used to solubilize each of theamphipathic compound, neoantigen and adjuvants, and the solubilizedcomponents are then mixed. Alternatively, the neoantigen, adjuvants andamphipathic compound may be mixed prior to solubilization, and thensolubilized together. In a further alternative, only one or more of theamphipathic compound, neoantigen or adjuvants are solubilized, and thenon-solubilized component(s) are added.

In a particular embodiment, to prepare the vaccine compositions theneoantigen and adjuvants are reconstituted together or separately insodium phosphate buffer with S100 lipids and cholesterol (Lipoid,Germany). These vaccine components are then lyophilized to form a drycake. Just prior to injection, the dry cake is resuspended in ISA51 VGoil (SEPPIC, France) to prepare a water-free oil-based vaccinecomposition.

In a particular embodiment, to prepare the vaccine compositions theneoantigen and adjuvants are reconstituted together or separately inacetate buffer (0.1M, pH 9.5) with DOPC and cholesterol (Lipoid,Germany). These vaccine components are then lyophilized to form a drycake. Just prior to injection, the dry cake is resuspended in ISA51 VGoil (SEPPIC, France) to prepare a water-free oil-based vaccinecomposition.

In another embodiment, to prepare the vaccine compositions a conjugatedneoantigen/T-helper epitope is reconstituted in 0.2% PEG-H₂O with lipidsDOPC and cholesterol (Lipoid, Germany). The polyI:C and lipid-basedadjuvants are reconstituted in water, and then added to theneoantigen-lipid mixture. These vaccine components are then lyophilizedto form a dry cake. Just prior to injection, the dry cake is resuspendedin ISA51 VG oil (SEPPIC, France) to prepare a water-free vaccinecomposition.

In the above embodiments, without being bound to a particular theory ofaction, it is believed that removal (drying) of the solvent leaves thevaccine components, including the neoantigen, in an array of amphipathiccompound molecules with their hydrophilic head groups oriented towardsthe vaccine components. The vaccine components and amphipathic compoundcan then be suspended in the hydrophobic carrier (such as oil) in theabsence of water, since they have been made sufficiently hydrophobic.

Additional components as described herein, such as T-helper epitope, maybe added at any stage in the formulation process. For instance, one ormore such additional components may be combined with the neoantigen,adjuvants and/or amphipathic compound either before or aftersolubilization, or added to the solubilized mixture. In anotherembodiment, the additional components may instead be added to orcombined with the dried mixture of neoantigen, adjuvants and amphipathiccompound, or combined with the hydrophobic carrier either before orafter resuspension of the dry mixture of neoantigen, adjuvants andamphipathic compound in the hydrophobic carrier. In an embodiment, theT-helper epitope is added to the vaccine composition in the same way asthe neoantigen. In an embodiment, the neoantigen and T-helper epitopeare a fused peptide.

In some embodiments, it may be appropriate to include an emulsifier inthe hydrophobic carrier to assist in stabilizing the vaccine componentsof the dry cake when they are resuspended in the hydrophobic carrier.The emulsifier is provided in an amount sufficient to resuspend the drymixture of neoantigen, adjuvants and amphipathic compound in thehydrophobic carrier and maintain the neoantigen, adjuvants andamphipathic compound in suspension in the hydrophobic carrier. Forexample, the emulsifier may be present at about 5% to about 15%weight/weight or weight/volume of the hydrophobic carrier.

Stabilizers such as sugars, anti-oxidants, or preservatives thatmaintain the biological activity or improve chemical stability toprolong the shelf life of any of the vaccine components, may be added tosuch compositions.

Embodiments

(1) A vaccine composition comprising:

-   -   (a) an amphipathic compound;    -   (b) a neoantigen; and    -   (c) a hydrophobic carrier.

(2) The composition of paragraph (1), wherein the composition iswater-free or substantially free of water.

(3) The composition of paragraph (2), wherein a composition that issubstantially free of water comprises less than about 10%, 9%, 8%, 7%,6%, 5%, 4%, 3%, 2%, 1%, 0.5%, 0.1%, 0.05% or 0.01% water on aweight/weight basis of the total weight of the carrier.

(4) The composition of any one of paragraphs (1) to (3), wherein theneoantigen is a neoantigenic peptide or a polynucleotide encoding aneoantigenic peptide.

(5) The composition of paragraph (4), wherein the neoantigenic peptideis 5 to 50 amino acids in length.

(6) The composition of paragraph (4) or (5), wherein the neoantigenicpeptide comprises one or more neoepitopes.

(7) The composition of paragraph (6), wherein the one or moreneoepitopes are selected from: an WIC class I T-cell neoepitope of 9 to11 amino acids in length; an WIC class II T-cell neoepitope of 13 to 17amino acids in length; or a B-cell neoepitope of 5 to 20 amino acids inlength.

(8) The composition of any one of paragraphs (1) to (7), wherein theneoantigen comprises the amino acid sequence PSKPSFQEFVDWENVSPELNSTDQPFL(SEQ ID NO: 2).

(9) The composition of paragraph (6) or (7), wherein at least one of theone or more neoepitopes is a patient-specific neoepitope.

(10) The composition of any one of paragraphs (1) to (9), whichcomprises one, two, three, four or five different neoantigens,optionally wherein each different neoantigen is derived from a differenttumor-specific antigen.

(11) The composition of paragraph (10), wherein each differentneoantigen comprises at least one patient-specific neoepitope from thesame patient.

(12) The composition of any one of paragraphs (1) to (11), wherein theneoantigen is a weakly immunogenic antigen.

(13) The composition of any one of paragraphs (1) to (12), wherein thecomposition comprises a low dose amount of the neoantigen.

(14) The composition of any one of paragraphs (1) to (13), wherein theneoantigen is sufficiently hydrophobic, or is made sufficientlyhydrophobic, such that the neoantigen is miscible in the hydrophobiccarrier.

(15) The composition of paragraph (14), wherein the neoantigen is madesufficiently hydrophobic by the presence of the amphipathic compound.

(16) The composition of paragraph (15), wherein the amphipathic compoundis closely associated with the neoantigen to make the neoantigenmiscible in the hydrophobic carrier.

(17) The composition of paragraph (16), wherein the amphipathic compoundforms a sheet or vesicular structure, partially or completelysurrounding the neoantigen.

(18) The composition of any one of paragraphs (1) to (17), wherein theamphipathic compound is a lipid, for example a phospholipid or a mixtureof phospholipids; optionally selected from dioleoyl phosphatidylcholine(DOPC), lecithin (e.g. Lipoid S100), or a mixture thereof.

(19) The composition of paragraph (18), wherein the lipids form a closedvesicular structure around the neoantigen, for example a single layervesicular structure (e.g. a micelle) or a bilayer vesicular structure(e.g. a unilamellar or multilamellar liposome).

(20) The composition of any one of paragraphs (1) to (19), wherein thehydrophobic carrier is an oil or a mixture of oils, optionally selectedfrom a vegetable oil, nut oil, mineral oil, or a mixture thereof.

(21) The composition of paragraph (20), wherein the hydrophobic carrieris mineral oil or is a mannide oleate in mineral oil solution, forexample Montanide® ISA 51.

(22) The composition of any one of paragraphs (1) to (21) furthercomprising an adjuvant.

(23) The composition of paragraph (22), wherein the adjuvant is apolyI:C polynucleotide adjuvant, a lipid-based adjuvant, a lipid A mimicor analog, or any combination thereof.

(24) The composition of paragraph (23), wherein the lipid-based adjuvantis PAM2Cys-Ser-(Lys)4 (SEQ ID NO: 4) or PAM3Cys-Ser-(Lys)4 (SEQ ID NO:4).

(25) The composition of any one of paragraphs (1) to (24) furthercomprising a T-helper epitope.

(26) The composition of paragraph (25), wherein the T-helper epitope isPADRE comprising the amino acid sequence AKXVAAWTLKAAA (SEQ ID NO: 6);Tetanus toxoid peptide F21E comprising the amino acid sequenceFNNFTVSFWLRVPKVSASHLE (SEQ ID NO: 7); or modified Tetanus toxin peptideA16L comprising the amino acid sequence AQYIKANSKFIGITEL (SEQ ID NO: 1).

(27) The composition of paragraph (26), wherein the T-helper epitope isoptionally conjugated or fused to the neoantigen.

(28) The composition of any one of paragraphs (1) to (27), whichcomprises:

-   -   (a) a lipid molecule mixture of        1,2-dioleoyl-sn-glycero-3-phosphocholine (DOPC) and cholesterol;    -   (b) a neoantigen;    -   (c) the hydrophobic carrier Montanide® ISA 51;    -   (d) a universal T-helper epitope from tetanus toxoid comprising        the amino acid sequence AQYIKANSKFIGITEL (SEQ ID NO: 1); and    -   (e) a polyI:C polynucleotide adjuvant.

(29) The composition of any one of paragraphs (1) to (28) for use ininducing an antibody immune response and/or a cell-mediated immuneresponse to the neoantigen in a subject.

(30) The composition of any one of paragraphs (1) to (29), whichgenerates an enhanced cell-mediated immune response that is at least2-fold, at least 3-fold, at least 4-fold, at least 5-fold, at least6-fold, at least 7-fold, at least 8-fold, at least 9-fold or at least10-fold greater than when the neoantigen is formulated in anaqueous-based vaccine formulation.

(31) The composition of paragraph 20, wherein the enhanced cell-mediatedimmune response is:

-   -   provided by only a single immunization with the composition;        and/or    -   provided by a low dose amount of the neoantigen in the        composition, wherein the low dose amount is about 50% of the        dose amount in the aqueous-based vaccine formulation.

(32) A method comprising administering the composition of any one ofparagraphs (1) to (31) to a subject in need thereof.

(33) The method according to paragraph (32), which is a method forinducing an antibody immune response and/or a cell-mediated immuneresponse to the neoantigen in the subject.

(34) The method of paragraph (33) which comprises only a singleadministration of the composition to the subject.

(35) The method of paragraph (33) or (34), wherein the compositioncomprises a low dose amount of the neoantigen.

(36) The method according to any one of paragraphs (33) to (35), whichis a method for the treatment and/or prevention of cancer.

(37) The method according to paragraph (36), wherein the compositioninduces a tumor-specific immune response in the treatment of the cancer.

(38) The method according to paragraph (37), wherein the compositioncomprises at least one patient-specific neoepitope and thetumor-specific immune response is patient-specific for the subject.

(39) The method according to any one of paragraphs (32) to (38), whichfurther comprises administering to the subject an agent that interfereswith DNA replication.

(40) The method according to paragraph (39), wherein the agent thatinterferes with DNA replication is cyclophosphamide.

(41) The method according to paragraph (40), which comprises a cycle oflow dose metronomic cyclophosphamide, wherein the cycle comprisesadministering the cyclophosphamide to the subject daily for a period of7 consecutive days, beginning every second week.

(42) The method according to any one of paragraphs (32) to (41), whichfurther comprises administering to the subject an immune responsecheckpoint inhibitor.

(43) The method according to paragraph (42), wherein the immune responsecheckpoint inhibitor is an inhibitor of Programmed Death-Ligand 1(PD-L1), Programmed Death 1 (PD-1), CTLA-4, PD-L2, LAG3, TIM3, 41BB,2B4, A2aR, B7H1, B7H3, B7H4, BTLA, CD2, CD27, CD28, CD30, CD40, CD70,CD80, CD86, CD160, CD226, CD276, DR3, GALS, GITR, HVEM, IDO1, IDO2,inducible T cell costimulatory (ICOS), KIR, LAIR1, LIGHT, macrophagereceptor with collageneous structure (MARCO), phosphatidylserine (PS),OX-40, SLAM, TIGIT, VISTA, VTCN1, or any combination thereof.

(44) Use of the composition of any one of paragraphs (1) to (31) forinducing an antibody immune response and/or a cell-mediated immuneresponse to said neoantigen in the subject.

(45) The use according to paragraph (44) which comprises only a singleadministration of the composition to the subject.

(46) The use according to paragraph (44) or (45), wherein thecomposition comprises a low dose amount of the neoantigen.

(47) The use according to any one of paragraphs (44) to (46), whereinthe antibody immune response and/or the cell-mediated immune response isa tumor-specific immune response.

(48) Use of the composition of any one of paragraphs (1) to (31) for thetreatment and/or prevention of cancer.

(49) The use according to paragraph (48) which comprises only a singleadministration of the composition to the subject.

(50) The use according to paragraph (48) or (49), wherein thecomposition comprises a low dose amount of the neoantigen.

(51) The use according to any one of paragraphs (44) to (50), whichfurther comprises use of an agent that interferes with DNA replicationand/or an immune response checkpoint inhibitor.

(52) The use according to paragraph (51), wherein the agent thatinterferes with DNA replication is cyclophosphamide.

(53) The use according to paragraph (51) or (52), wherein the immuneresponse checkpoint inhibitor is an inhibitor of Programmed Death-Ligand1 (PD-L1), Programmed Death 1 (PD-1), CTLA-4, PD-L2, LAG3, TIM3, 41BB,2B4, A2aR, B7H1, B7H3, B7H4, BTLA, CD2, CD27, CD28, CD30, CD40, CD70,CD80, CD86, CD160, CD226, CD276, DR3, GALS, GITR, HVEM, IDO1, IDO2,inducible T cell costimulatory (ICOS), KIR, LAIR1, LIGHT, macrophagereceptor with collageneous structure (MARCO), phosphatidylserine (PS),OX-40, SLAM, TIGIT, VISTA, VTCN1, or any combination thereof.

(54) A kit comprising: a first container comprising an amphipathiccompound and a neoantigen; and a second container comprising ahydrophobic carrier.

(55) The kit of paragraph (54), wherein the amphipathic compound in thefirst container comprise 1,2-dioleoyl-sn-glycero-3-phosphocholine (DOPC)and cholesterol.

(56) The kit of paragraph (55) or (56), wherein the first containerfurther comprises a T-helper epitope.

(57) The kit of paragraph (56), wherein the T-helper epitope is apeptide comprising the amino acid sequence AQYIKANSKFIGITEL (SEQ ID NO:1).

(58) The kit of any one of paragraphs (54) to (57), wherein the firstcontainer further comprises an adjuvant.

(59) The kit of paragraph (58), wherein the adjuvant is a polyI:Cpolynucleotide.

(60) The kit of any one of paragraphs (54) to (59), wherein thecomponents of the first container were subject to lyophilization to forma dry cake.

(61) The kit of any one of paragraphs (54) to (60), for use in inducingan antibody immune response and/or a cell-mediated immune response tothe neoantigen in a subject.

(62) The kit of any one of paragraphs (54) to (61) which comprises asufficient amount of the components for only a single administration.

(63) The kit of any one of paragraphs (54) to (62), wherein the kitcomprises a low dose amount of the neoantigen.

The invention is further illustrated by the following non-limitingexamples.

EXAMPLES Example 1

i) Identification and Synthesis of Neoantigens

To identify neoantigens, the whole exome of a tumor is sequenced (RNAand/or genomic DNA) and screened against normal tissue genome,preferably from the same patient. This is performed using nextgeneration sequencing. Somatic gene mutations are identified bycomparing tumor and normal genome sequences. Mutations can arise frommissense mutations or an insertion/deletion. Genes with mutations aretranslated to the protein sequence which is then screened in silicousing an algorithm (e.g. NetMHC, NetMHCpan, MHCFlurry, IEDB) that canpredict peptide sequences likely to bind to patient HLA. From thesealgorithms, peptides are selected based on their affinity for MHCbinding, whether they are naturally processed and presented andprediction of mutation functional impact using in silico algorithm (e.g.SIFT, POLYPHEN). Peptides are sequenced by a contract manufacturer underGMP conditions.

ii) Formulation in DepoVax (DPX)

To prepare vaccines, peptide mixture and adjuvants are firstreconstituted in an appropriate aqueous buffer (e.g. acetate buffer,sodium phosphate, sodium bicarbonate, phosphate buffered saline) withDOPC and cholesterol (Lipoid, Germany). This preparation is thenlyophilized to form a dry cake. Just prior to injection, the dry cake isreconstituted in an oil (e.g. ISA51 VG). Extra vials are prepared formoisture analysis and reconstitution testing.

iii) Animal Testing

Since neoantigen vaccines are uniquely and individually prepared foreach patient, they cannot be tested in advance using animal models.Instead, it is possible to perform proof-of-concept using neoantigensderived from murine tumors (e.g. MethA, Bl6F10, etc.).

iv) Clinical Testing

Patient specific neoantigen vaccines are prepared using the methodsdescribed herein and administered to patients with or without concurrenttreatment with immune modulators, such as metronomic cyclophosphamide orcheckpoint inhibitors. Immunogenicity is monitored using IFN-gammaELISPOT assay with PBMCs isolated from patients at regular intervalsthroughout the study. Immunogenicity can also be monitored using custompeptide-WIC multimer reagents to stain cells for flow cytometry.

Example 2

Pathogen free, C57BL/6 VAF/Elite® Crl mice, 6-8 weeks of age, werepurchased from Charles River Laboratories (St. Constant, PQ) and housedaccording to institutional guidelines with water and food ad libitumunder filter controlled air circulation. The neoantigen Mut30(PSKPSFQEFVDWENVSPELNSTDQPFL; SEQ ID NO: 2) was identified from Castle2012 and was synthesized by Genscript.

The immunogenicity of the Mut30 peptide prepared in either an oil-basedformulation or an aqueous formulation was compared. The formulationscontained a DNA or RNA based poly I:C molecule as an adjuvant.

To prepare the oil-based formulations, the Mut30 peptide, polyI:Cadjuvant (DNA or RNA) and T-helper epitope (A16L peptide) were firstreconstituted in an acetate buffer (0.1M, pH 9.5) with DOPC andcholesterol (Lipoid, Germany). The vaccine components were thenlyophilized to form a dry cake. Just prior to injection, the dry cakewas reconstituted in ISA51 VG oil (SEPPIC, France).

To prepare the aqueous-based formulations, the Mut30 peptide, polyI:Cadjuvant (DNA or RNA) and T-helper epitope (A16L peptide) wereformulated in 0.05M sodium acetate buffer at pH 10±1.

Mice in group 1 (n=6) were vaccinated with 100 microliters of an aqueousbuffered formulation containing 100 micrograms of Mut30 neoantigen, 50micrograms of A16L peptide and 40 micrograms of DNA-based poly I:C in0.05M sodium acetate buffer at pH 6±1.

Mice in group 2 (n=6) were vaccinated with 100 microliters of an aqueousbuffered formulation containing 100 micrograms of Mut30 neoantigen, 50micrograms of A16L peptide and 40 micrograms of RNA-based poly I:C in0.05M sodium acetate buffer at pH 6±1.

Mice in group 3 (n=6) were vaccinated with 100 microliters of anoil-based depot vaccine containing 100 micrograms of Mut30 neoantigen,50 micrograms of A16L peptide, 40 micrograms of DNA-based poly I:C, 12milligrams of DOPC and 1.2 milligrams of cholesterol.

Mice in group 4 (n=6) were vaccinated with 100 microliters of anoil-based depot vaccine containing 100 micrograms of Mut30 neoantigen,50 micrograms of A16L peptide, 40 micrograms of RNA-based poly I:C, 12milligrams of DOPC and 1.2 milligrams of cholesterol.

Mice in group 5 (n=1) were not vaccinated.

Eight days after vaccination, mice were terminated and spleenscollected. Splenocytes were stimulated in an IFN-gamma ELISPOT plate (BDBiosciences) with syngeneic dendritic cells unloaded (background) orloaded with an irrelevant peptide (RAHYNIVTF; SEQ ID NO: 8) or Mut30antigen. After 18 hours of culture, plates were developed and the numberof spot forming units (SFU) counted using Immunospot Reader (C.T.L.).The results are shown in FIG. 1 as average response±SEM. Statisticalanalysis was performed by 2-way ANOVA with Bonferroni post testcomparing group responses to Mut30 peptide: *p<0.05, ***p<0.001.

The results demonstrate that the oil-based depot forming vaccinesgenerate statistically significant stronger immune responses toneoantigen peptide after a single immunization compared to aqueous,non-depot forming vaccine formulations with identical components.

Example 3

Pathogen free, C57BL/6 VAF/Elite® Crl mice, 6-8 weeks of age, werepurchased from Charles River Laboratories (St. Constant, PQ) and housedaccording to institutional guidelines with water and food ad libitumunder filter controlled air circulation. The neoantigen Mut30(PSKPSFQEFVDWENVSPELNSTDQPFL; SEQ ID NO: 2) was identified from Castle2012 and synthesized by Genscript.

Oil-based depot vaccine formulations were prepared with Mut30 antigen ata higher (100 micrograms) and lower (50 micrograms) dose.

To prepare the oil-based formulations, the Mut30 peptide (low or highdose amount), polyI:C adjuvant (DNA or RNA) and T-helper epitope (A16Lpeptide) were first reconstituted in an acetate buffer (0.1M, pH 9.5)with DOPC and cholesterol (Lipoid, Germany). The vaccine components werethen lyophilized to form a dry cake. Just prior to injection, the drycake was reconstituted in ISA51 VG oil (SEPPIC, France).

Mice in group 1 (n=6) were vaccinated with 100 microliters of anoil-based depot vaccine containing 100 micrograms of Mut30 neoantigen,50 micrograms of A16L peptide, 40 micrograms of DNA-based poly I:C, 12milligrams of DOPC and 1.2 milligrams of cholesterol.

Mice in group 2 (n=6) were vaccinated with 100 microliters of anoil-based depot vaccine containing 100 micrograms of Mut30 neoantigen,50 micrograms of A16L peptide, 40 micrograms of RNA-based poly I:C, 12milligrams of DOPC and 1.2 milligrams of cholesterol.

Mice in group 3 (n=6) were vaccinated with 100 microliters of anoil-based depot vaccine containing 50 micrograms of Mut30 neoantigen, 50micrograms of A16L peptide, 40 micrograms of DNA-based poly I:C, 12milligrams of DOPC and 1.2 milligrams of cholesterol.

Mice in group 4 (n=6) were vaccinated with 100 microliters of anoil-based depot vaccine containing 50 micrograms of Mut30 neoantigen, 50micrograms of A16L peptide, 40 micrograms of RNA-based poly I:C, 12milligrams of DOPC and 1.2 milligrams of cholesterol.

Mice in group 5 (n=1) were not vaccinated.

Eight days after vaccination, mice were terminated and spleenscollected. Splenocytes were stimulated in an IFN-gamma ELISPOT plate (BDBiosciences) with syngeneic dendritic cells unloaded (background) orloaded with an irrelevant peptide (RAHYNIVTF; SEQ ID NO: 8) or Mut30neoantigen. After 18 hours of culture, plates were developed and thenumber of spot forming units (SFU) counted using Immunospot Reader(C.T.L.). The results are shown in FIG. 2 as average response±SEM.Statistical analysis was performed by 2-way ANOVA with Bonferroni posttest comparing group responses to Mut30 peptide. No statisticallysignificant difference was observed between groups comparing high (100micrograms) and low (50 micrograms) doses of Mut30 neoantigen with bothDNA-based poly I:C and RNA-based poly I:C.

The results demonstrate that the oil-based depot forming vaccinesgenerate comparable immune responses to neoantigen peptide at high (100micrograms) and lower (50 micrograms) dose of antigen after a singleimmunization.

Example 4

Pathogen free, C57BL/6NCrl mice, 6-8 weeks of age, were purchased fromCharles River Laboratories (St. Constant, PQ) and housed according toinstitutional guidelines with water and food ad libitum under filtercontrolled air circulation. The neoantigen Mut30(PSKPSFQEFVDWENVSPELNSTDQPFL; SEQ ID NO: 2) was identified from Castle2012 and was synthesized by Genscript.

Two oil-based formulations were prepared with a RNA or DNA based polyI:C molecule and were compared to an aqueous buffer vaccine containingRNA based poly I:C. The aqueous buffer vaccine was designed to mimic theformulation described in Castle 2012.

To prepare the oil-based formulations, the Mut30 peptide, polyI:Cadjuvant (DNA or RNA) and T-helper epitope (A16L peptide) were firstreconstituted in an acetate buffer (0.1M, pH 9.5) with DOPC andcholesterol (Lipoid, Germany). The vaccine components were thenlyophilized to form a dry cake. Just prior to injection, the dry cakewas reconstituted in ISA51 VG oil (SEPPIC, France).

To prepare the aqueous-based formulations, the Mut30 peptide andRNA-based polyI:C adjuvant were formulated in 0.1M phosphate bufferedsaline at pH 10.0±1.

Mice in group 1 (n=5) were vaccinated with 100 microliters of an aqueousbuffered formulation containing 100 micrograms of Mut30 neoantigen and100 micrograms of RNA-based poly I:C in 0.05M sodium acetate buffer atpH 6.0.

Mice in group 2 (n=5) were vaccinated with 100 microliters of anoil-based depot vaccine containing 50 micrograms of Mut30 neoantigen, 50micrograms of A16L peptide, 40 micrograms of RNA-based poly I:C, 12milligrams of DOPC and 1.2 milligrams of cholesterol.

Mice in group 3 (n=4) were vaccinated with 100 microliters of anoil-based depot vaccine containing 50 micrograms of Mut30 neoantigen, 50micrograms of A16L peptide, 40 micrograms of DNA-based poly I:C, 12milligrams of DOPC and 1.2 milligrams of cholesterol.

Mice in group 4 (n=1) were not vaccinated.

Eight days after vaccination, mice were terminated and spleenscollected. Splenocytes were stimulated in an IFN-gamma ELISPOT plate (BDBiosciences) with syngeneic dendritic cells unloaded (background) orloaded with an irrelevant peptide (EGPRNQDWL; SEQ ID NO: 9) or Mut30neoantigen. After 18 hours of culture, plates were developed and thenumber of spot forming units (SFU) counted using Immunospot Reader(C.T.L.). The results are shown in FIG. 3 as average response±SEM.Statistical analysis was performed by 2-way ANOVA with Bonferroni posttest comparing group responses to Mut30 peptide, *p<0.05, ***p<0.001.

The results demonstrate that the oil-based depot forming vaccinegenerates stronger immune responses to neoantigen peptides after asingle immunization compared to an aqueous, non-depot forming vaccine.

All publications and patent applications cited in this specification areherein incorporated by reference as if each individual publication orpatent application were specifically and individually indicated to beincorporated by reference. The citation of any publication is for itsdisclosure prior to the filing date and should not be construed as anadmission that the present invention is not entitled to antedate suchpublication by virtue of prior invention.

Although the foregoing invention has been described in some detail byway of illustration and example for purposes of clarity ofunderstanding, it is readily apparent to those of ordinary skill in theart in light of the teachings of this invention that certain changes andmodifications may be made thereto without departing from the spirit orscope of the appended claims.

It must be noted that as used in this specification and the appendedclaims, the singular forms “a,” “an,” and “the” include plural referenceunless the context clearly dictates otherwise. Unless defined otherwiseall technical and scientific terms used herein have the same meaning ascommonly understood to one of ordinary skill in the art to which thisinvention belongs.

The phrase “and/or,” as used herein in the specification and in theclaims, should be understood to mean “either or both” of the elements soconjoined, i.e., elements that are conjunctively present in some casesand disjunctively present in other cases. Multiple elements listed with“and/or” should be construed in the same fashion, i.e., “one or more” ofthe elements so conjoined. Other elements may optionally be presentother than the elements specifically identified by the “and/or” clause,whether related or unrelated to those elements specifically identified.Thus, as a non-limiting example, a reference to “A and/or B”, when usedin conjunction with open-ended language such as “comprising” can refer,in one embodiment, to A only (optionally including elements other thanB); in another embodiment, to B only (optionally including elementsother than A); in yet another embodiment, to both A and B (optionallyincluding other elements); etc.

As used herein in the specification and in the claims, “or” should beunderstood to encompass the same meaning as “and/or” as defined above.For example, when separating items in a list, “or” or “and/or” shall beinterpreted as being inclusive, i.e., the inclusion of at least one, butalso including more than one, of a number or list of elements, and,optionally, additional unlisted items.

As used herein, whether in the specification or the appended claims, thetransitional terms “comprising”, “including”, “carrying”, “having”,“containing”, “involving”, and the like are to be understood as beinginclusive or open-ended (i.e., to mean including but not limited to),and they do not exclude unrecited elements, materials or method steps.Only the transitional phrases “consisting of” and “consistingessentially of”, respectively, are closed or semi-closed transitionalphrases with respect to claims and exemplary embodiment paragraphsherein. The transitional phrase “consisting of” excludes any element,step, or ingredient which is not specifically recited. The transitionalphrase “consisting essentially of” limits the scope to the specifiedelements, materials or steps and to those that do not materially affectthe basic characteristic(s) of the invention disclosed and/or claimedherein.

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1-41. (canceled)
 42. A vaccine composition comprising: (a) anamphipathic compound selected from a phospholipid or a mixture ofphospholipids; (b) a neoantigen; (c) a hydrophobic carrier selected froman oil, a mixture of oils, or a mannide oleate in mineral oil solution;(d) a T-helper epitope; and (e) a polyI:C polynucleotide adjuvant. 43.The composition of claim 42, wherein the composition is water-free orsubstantially free of water, wherein a composition that is substantiallyfree of water comprises less than about 10%, 9%, 8%, 7%, 6%, 5%, 4%, 3%,2%, 1%, 0.5%, 0.1%, 0.05% or 0.01% water on a weight/weight basis of thetotal weight of the carrier.
 44. The composition of claim 42, whereinthe neoantigen is a neoantigenic peptide or a polynucleotide encoding aneoantigenic peptide.
 45. The composition of claim 44, wherein theneoantigenic peptide is 5 to 50 amino acids in length.
 46. Thecomposition of claim 44, wherein the neoantigenic peptide comprises oneor more neoepitopes.
 47. The composition of claim 46, wherein the one ormore neoepitopes are selected from: an MHC class I T-cell neoepitope of9 to 11 amino acids in length; an MHC class II T-cell neoepitope of 13to 17 amino acids in length; or a B-cell neoepitope of 5 to 20 aminoacids in length.
 48. The composition of claim 42, wherein the neoantigencomprises the amino acid sequence PSKPSFQEFVDWENVSPELNSTDQPFL (SEQ IDNO: 2).
 49. The composition of claim 42, wherein the neoantigen is aweakly immunogenic antigen.
 50. The composition of claim 42, wherein thecomposition comprises a low dose amount of the neoantigen.
 51. Thecomposition of claim 42, wherein the neoantigen is sufficientlyhydrophobic, or is made sufficiently hydrophobic, such that theneoantigen is miscible in the hydrophobic carrier.
 52. The compositionof claim 51, wherein the neoantigen is made sufficiently hydrophobic bythe presence of the amphipathic compound, wherein: the amphipathiccompound is closely associated with the neoantigen to make theneoantigen miscible in the hydrophobic carrier; and/or the amphipathiccompound forms a sheet or vesicular structure, partially or completelysurrounding the neoantigen.
 53. The composition of claim 42, wherein thecomposition further comprises cholesterol.
 54. The composition of claim42, wherein the polyI:C polynucleotide adjuvant is a DNA and/or RNApolyI:C polynucleotide adjuvant.
 55. The composition of claim 42,wherein the T-helper epitope is PADRE comprising the amino acid sequenceAKXVAAWTLKAAA (SEQ ID NO: 6); Tetanus toxoid peptide F21E comprising theamino acid sequence FNNFTVSFWRVPKVSASHLE (SEQ ID NO: 7); or modifiedTetanus toxin peptide A16L comprising the amino acid sequenceAQYIKANSKFIGITEL (SEQ ID NO: 1).
 56. The composition of claim 42, whichcomprises: (a) a lipid molecule mixture of1,2-dioleoyl-sn-glycero-3-phosphocholine (DOPC) and cholesterol; (b) aneoantigen; (c) mannide oleate in mineral oil solution; (d) a universalT-helper epitope from tetanus toxoid comprising the amino acid sequenceAQYIKANSKFIGITEL (SEQ ID NO: 1); and (e) a polyI:C polynucleotideadjuvant.
 57. The composition of claim 42, which generates an enhancedcell-mediated immune response that is at least 2-fold, at least 3-fold,at least 4-fold, at least 5-fold, at least 6-fold, at least 7-fold, atleast 8-fold, at least 9-fold or at least 10-fold greater than when theneoantigen is formulated in an aqueous-based vaccine formulation. 58.The composition of claim 57, wherein the enhanced cell-mediated immuneresponse is provided by only a single immunization with the composition.59. The composition of claim 57, wherein the enhanced cell-mediatedimmune response is provided by a low dose amount of the neoantigen inthe composition, wherein the low dose amount is about 50% of the doseamount in the aqueous-based vaccine formulation.
 60. A method forinducing an antibody immune response and/or a cell-mediated immuneresponse to a neoantigen, said method comprising administering thecomposition of claim 42 to a subject in need thereof.
 61. The method ofclaim 60 which comprises only a single administration of the compositionto the subject.
 62. The method of claim 60, wherein the compositioncomprises a low dose amount of the neoantigen.
 63. The method accordingto claim 60, which is a method for the treatment and/or prevention ofcancer.
 64. The method according to claim 60, which further comprisesadministering to the subject an agent that interferes with DNAreplication and/or an immune response checkpoint inhibitor.
 65. Themethod according to claim 64, wherein the agent that interferes with DNAreplication is cyclophosphamide and the immune response checkpointinhibitor is an inhibitor of Programmed Death-Ligand 1 (PD-L1),Programmed Death 1 (PD-1), CTLA-4, PD-L2, LAG3, 41BB, 2B4, A2aR, B7H1,B7H3, B7H4, BTLA, CD2, CD27, CD28, CD30, CD40, CD70, CD80, CD86, CD160,CD226, CD276, DR3, GALS, GITR, HVEM, IDO1, IDO2, inducible T cellcostimulatory (ICOS), KIR, LAIR1, LIGHT, macrophage receptor withcollageneous structure (MARCO), phosphatidylserine (PS), OX-40, SLAM,TIGIT, VISTA, VTCN1, or any combination thereof.
 66. A kit comprising: afirst container comprising an amphipathic compound selected from aphospholipid or a mixture of phospholipids, a T-helper epitope, apolyI:C polynucleotide adjuvant, and a neoantigen; and a secondcontainer comprising a hydrophobic carrier selected from an oil, amixture of oils, or a mannide oleate in mineral oil solution.